83 FR 5433 - Agency Information Collection Activities; Proposed Collection; Comment Request; Survey on the Occurrence of Foodborne Illness Risk Factors in Selected Retail and Foodservice Facility Types
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration Federal Register Volume 83, Issue 26 (February 7, 2018)
Food and Drug Administration
Federal Register Volume 83, Issue 26 (February 7, 2018)
| Page Range | 5433-5436 | |
| FR Document | 2018-02414 |
[Federal Register Volume 83, Number 26 (Wednesday, February 7, 2018)] [Notices] [Pages 5433-5436] From the Federal Register Online [www.thefederalregister.org] [FR Doc No: 2018-02414] ----------------------------------------------------------------------- DEPARTMENT OF HEALTH AND HUMAN SERVICES Food and Drug Administration [Docket No. FDA-2012-N-0547] Agency Information Collection Activities; Proposed Collection; Comment Request; Survey on the Occurrence of Foodborne Illness Risk Factors in Selected Retail and Foodservice Facility Types AGENCY: Food and Drug Administration, HHS. ACTION: Notice. ----------------------------------------------------------------------- SUMMARY: The Food and Drug Administration (FDA or Agency) is announcing an opportunity for public comment on the proposed collection of certain information by the Agency. Under the Paperwork Reduction Act of 1995 (PRA), Federal Agencies are required to publish notice in the Federal Register concerning each proposed collection of information, including each proposed extension of an existing collection of information, and to allow 60 days for public comment in response to the notice. This notice solicits comments on ``Survey on the Occurrence of Foodborne Illness Risk Factors in Selected Retail and Foodservice Facility Types.'' DATES: Submit either electronic or written comments on the collection of information by April 9, 2018. ADDRESSES: You may submit comments as follows. Please note that late, untimely filed comments will not be considered. Electronic comments must be submitted on or before April 9, 2018. The https://www.regulations.gov electronic filing system will accept comments until midnight Eastern Time at the end of April 9, 2018. Comments received by mail/hand delivery/courier (for written/paper submissions) will be considered timely if they are postmarked or the delivery service acceptance receipt is on or before that date. Electronic Submissions Submit electronic comments in the following way:Federal eRulemaking Portal: https://www.regulations.gov. Follow the instructions for submitting comments. Comments submitted electronically, including attachments, to https://www.regulations.gov will be posted to the docket unchanged. Because your comment will be made public, you are solely responsible for ensuring that your comment does not include any confidential information that you or a third party may not wish to be posted, such as medical information, your or anyone else's Social Security number, or confidential business information, such as a manufacturing process. Please note that if you include your name, contact information, or other information that identifies you in the body of your comments, that information will be posted on https://www.regulations.gov. If you want to submit a comment with confidential information that you do not wish to be made available to the public, submit the comment as a written/paper submission and in the manner detailed (see ``Written/Paper Submissions'' and ``Instructions''). Written/Paper Submissions Submit written/paper submissions as follows: Mail/Hand delivery/Courier (for written/paper submissions): Dockets Management Staff (HFA-305), Food and Drug Administration, 5630 Fishers Lane, Rm. 1061, Rockville, MD 20852. For written/paper comments submitted to the Dockets Management Staff, FDA will post your comment, as well as any attachments, except for information submitted, marked and identified, as confidential, if submitted as detailed in ``Instructions.'' Instructions: All submissions received must include the Docket No. FDA-2012-N-0547 for ``Survey on the Occurrence of Foodborne Illness Risk Factors in Selected Retail and Foodservice Facility Types.'' Received comments, those filed in a timely manner (see ADDRESSES), will be placed in the docket and, except for those submitted as ``Confidential Submissions,'' publicly viewable at https://www.regulations.gov or at the Dockets Management Staff between 9 a.m. and 4 p.m., Monday through Friday. Confidential Submissions--To submit a comment with confidential information that you do not wish to be made publicly available, submit your comments only as a written/paper submission. You should submit two copies total. One copy will include the information you claim to be confidential with a heading or cover note that states ``THIS DOCUMENT CONTAINS CONFIDENTIAL INFORMATION.'' The Agency will review this copy, including the claimed confidential information, in its consideration of comments. The second copy, which will have the claimed confidential information redacted/blacked out, will be available for public viewing and posted on https://www.regulations.gov. Submit both copies to the Dockets Management Staff. If you do not wish your name and contact information to be made publicly available, you can provide this information on the cover sheet and not in the body of your comments and you must identify this information as ``confidential.'' Any information marked as ``confidential'' will not be disclosed except in accordance with 21 CFR 10.20 and other applicable disclosure law. For more information about FDA's posting of comments to public dockets, see 80 FR 56469, September 18, 2015, or access the information at: https://www.thefederalregister.org/fdsys/pkg/FR-2015-09-18/pdf/2015-23389.pdf. Docket: For access to the docket to read background documents or the electronic and written/paper comments received, go to https://www.regulations.gov and insert the docket number, found in brackets in the heading of this document, into the ``Search'' box and follow the prompts and/or go to the Dockets Management Staff, 5630 Fishers Lane, Rm. 1061, Rockville, MD 20852. FOR FURTHER INFORMATION CONTACT: Ila S. Mizrachi, Office of Operations, Food and Drug Administration, Three White Flint North, 10A-12M, 11601 Landsdown St., North Bethesda, MD 20852, 301-796-7726, [email protected]. SUPPLEMENTARY INFORMATION: Under the PRA (44 U.S.C. 3501-3520), Federal Agencies must obtain approval from the Office of Management and Budget (OMB) for each collection of information they conduct or sponsor. ``Collection of information'' is defined in 44 U.S.C. 3502(3) and 5 CFR 1320.3(c) and includes Agency requests or requirements that members of the public submit reports, keep records, or provide information to a third party. Section 3506(c)(2)(A) of the PRA (44 U.S.C. 3506(c)(2)(A)) requires Federal Agencies to provide a 60-day notice in the Federal Register concerning each [[Page 5434]] proposed collection of information, including each proposed extension of an existing collection of information, before submitting the collection to OMB for approval. To comply with this requirement, FDA is publishing notice of the proposed collection of information set forth in this document. With respect to the following collection of information, FDA invites comments on these topics: (1) Whether the proposed collection of information is necessary for the proper performance of FDA's functions, including whether the information will have practical utility; (2) the accuracy of FDA's estimate of the burden of the proposed collection of information, including the validity of the methodology and assumptions used; (3) ways to enhance the quality, utility, and clarity of the information to be collected; and (4) ways to minimize the burden of the collection of information on respondents, including through the use of automated collection techniques, when appropriate, and other forms of information technology. Survey on the Occurrence of Foodborne Illness Risk Factors in Selected Retail and Foodservice Facility Types OMB Control Number 0910-0744--Extension I. Background From 1998 to 2008, FDA's National Retail Food Team conducted a study to measure trends in the occurrence of foodborne illness risk factors, preparation practices, and employee behaviors most commonly reported to the Centers for Disease Control and Prevention as contributing factors to foodborne illness outbreaks at the retail level. Specifically, data was collected by FDA Specialists in retail and foodservice establishments at 5-year intervals (1998, 2003, and 2008) to observe and document trends in the occurrence of the following foodborne illness risk factors: Food from Unsafe Sources, Poor Personal Hygiene, Inadequate Cooking, Improper Holding/Time and Temperature, and Contaminated Equipment/Cross-Contamination. FDA developed reports summarizing the findings for each of the three data collection periods (1998, 2003, and 2008) (Refs. 1 to 3). Data from all three data collection periods were analyzed to detect trends in improvement or regression over time and to determine whether progress had been made toward the goal of reducing the occurrence of foodborne illness risk factors in selected retail and foodservice facility types (Ref. 4). Using this 10-year survey as a foundation, in 2013-2014, FDA initiated a new study in full service and fast food restaurants. This study will span 10 years with a data collection currently being conducted in 2017-2018 and another data collection planned for 2021- 2022 (the subject of this information collection request extension). Table 1--Description of the Facility Types Included in the Survey ------------------------------------------------------------------------ Facility type Description ------------------------------------------------------------------------ Full Service Restaurants.......... A restaurant where customers place their order at their table, are served their meal at the table, receive the service of the wait staff, and pay at the end of the meal. Fast Food Restaurants............. A restaurant that is not a full service restaurant. This includes restaurants commonly referred to as quick service restaurants and fast casual restaurants. ------------------------------------------------------------------------ The purpose of the study is to: Assist FDA with developing retail food safety initiatives and policies focused on the control of foodborne illness risk factors; Identify retail food safety work plan priorities and allocate resources to enhance retail food safety nationwide; Track changes in the occurrence of foodborne illness risk factors in retail and foodservice establishments over time; and Inform recommendations to the retail and foodservice industry and State, local, tribal, and territorial regulatory professionals on reducing the occurrence of foodborne illness risk factors. The statutory basis for FDA conducting this study is derived from the Public Health Service Act (PHS Act) (42 U.S.C. 243, section 311(a)). Responsibility for carrying out the provisions of the PHS Act relative to food protection was transferred to the Commissioner of Food and Drugs in 1968 (21 CFR 5.10(a)(2) and (4)). Additionally, the Federal Food, Drug, and Cosmetic Act (21 U.S.C. 301 et seq.) and the Economy Act (31 U.S.C. 1535) require FDA to provide assistance to other Federal, State, and local government bodies. The objectives of the study are to: Identify the least and most often occurring foodborne illness risk factors and food safety behaviors/practices in retail and foodservice facility types during each data collection period; Track improvement and/or regression trends in the occurrence of foodborne illness risk factors during the 10-year study period; Examine potential correlations between operational characteristics of food establishments and the control of foodborne illness risk factors; Examine potential correlations between elements within regulatory retail food protection programs and the control of foodborne illness risk factors; and Determine the extent to which food safety management systems and the presence of a certified food protection manager impact the occurrence of foodborne illness risk factors. The methodology to be used for this information collection is described as follows. To obtain a sufficient number of observations to conduct statistically significant analysis, FDA will conduct approximately 400 data collections in each facility type. This sample size has been calculated to provide for sufficient observations to be 95 percent confident that the compliance percentage is within 5 percent of the true compliance percentage. A geographical information system database containing a listing of businesses throughout the United States provides the establishment inventory for the data collections. FDA samples establishments from the inventory based on the descriptions in table 1. FDA does not intend to sample operations that handle only prepackaged food items or conduct low-risk food preparation activities. The ``FDA Food Code'' contains a grouping of establishments by risk, based on the type of food preparation that is normally conducted within the operation (Ref. 5). The intent is to sample establishments that fall under risk categories 2 through 4. FDA has approximately 25 Retail Food Specialists (Specialists) who serve as the data collectors for the 10-year study. The Specialists are geographically dispersed throughout the [[Page 5435]] United States and possess technical expertise in retail food safety and a solid understanding of the operations within each of the facility types to be surveyed. The Specialists are also standardized by FDA's Center for Food Safety and Applied Nutrition personnel in the application and interpretation of the FDA Food Code (Ref. 5). Sampling zones have been established that are equal to the 150-mile radius around a Specialist's home location. The sample is selected randomly from among all eligible establishments located within these sampling zones. The Specialists are generally located in major metropolitan areas (i.e., population centers) across the contiguous United States. Population centers usually contain a large concentration of the establishments FDA intends to sample. Sampling from the 150-mile radius sampling zones around the Specialists' home locations provides three advantages to the study: 1. It provides a cross section of urban and rural areas from which to sample the eligible establishments. 2. It represents a mix of small, medium, and large regulatory entities having jurisdiction over the eligible establishments. 3. It reduces overnight travel and therefore reduces travel costs incurred by the Agency to collect data. The sample for each data collection period is evenly distributed among Specialists. Given that participation in the study by industry is voluntary and the status of any given randomly selected establishment is subject to change, substitute establishments have been selected for each Specialist for cases where the restaurant facility is misclassified, closed, or otherwise unavailable, unable, or unwilling to participate. Prior to conducting the data collection, Specialists contact the State or local jurisdiction that has regulatory responsibility for conducting retail food inspections for the selected establishment. The Specialist verifies with the jurisdiction that the facility has been properly classified for the purposes of the study and is still in operation. The Specialist ascertains whether the selected facility is under legal notice from the State or local regulatory authority. If the selected facility is under legal notice, the Specialist will not conduct a data collection, and a substitute establishment will be used. An invitation is extended to the State or local regulatory authority to accompany the Specialist on the data collection visit. A standard form is used by the Specialists during each data collection. The form is divided into three sections: Section 1-- ``Establishment Information''; Section 2--``Regulatory Authority Information''; and Section 3--``Foodborne Illness Risk Factor and Food Safety Management System Assessment.'' The information in Section 1-- ``Establishment Information'' of the form is obtained during an interview with the establishment owner or person in charge by the Specialist and includes a standard set of questions. The information in Section 2--``Regulatory Authority Information'' is obtained during an interview with the program director of the State or local jurisdiction that has regulatory responsibility for conducting inspections for the selected establishment. Section 3 includes three parts: Part A for tabulating the Specialists' observations of the food employees' behaviors and practices in limiting contamination, proliferation, and survival of food safety hazards; Part B for assessing the food safety management system being implemented by the facility; and Part C for assessing the frequency and extent of food employee hand washing. The information in Part A is collected from the Specialists' direct observations of food employee behaviors and practices. Infrequent, nonstandard questions may be asked by the Specialists if clarification is needed on the food safety procedure or practice being observed. The information in Part B is collected by making direct observations and asking follow up questions of facility management to obtain information on the extent to which the food establishment has developed and implemented food safety management systems. The information in Part C is collected by making direct observations of food employee hand washing. No questions are asked in the completion of Section 3, Part C of the form. FDA collects the following information associated with the establishment's identity: Establishment name, street address, city, state, zip code, county, industry segment, and facility type. The establishment identifying information is collected to ensure the data collections are not duplicative. Other information related to the nature of the operation, such as seating capacity and number of employees per shift, is also collected. Data will be consolidated and reported in a manner that does not reveal the identity of any establishment included in the study. FDA has collaborated with the Food Protection and Defense Institute to develop a web-based platform in FoodSHIELD to collect, store, and analyze data for the Retail Risk Factor Study. This platform is accessible to State, local, territorial, and tribal regulatory jurisdictions to collect data relevant to their own risk factor studies. For the 2015-2016 data collection, FDA piloted the use of hand-held technology for capturing the data onsite during the data collection visits. The tablets that were made available for the data collections were part of a broader Agency initiative focused on internal uses of hand-held technology. The tablets provided for the data collection presented several technical and logistical challenges and increased the time burden associated with the data collection as compared to the manual entry of data collections. FDA continues to assess the feasibility for fully incorporating use of hand-held technology in subsequent data collections during the 10-year study period. When a data collector is assigned a specific establishment, he or she conducts the data collection and enters the information into the web-based data platform. The interface will support the manual entering of data, as well as the ability to directly enter information in the database via a web browser. The burden for the 2021-2022 data collection is as follows. For each data collection, the respondents will include: (1) The person in charge of the selected facility (whether it be a fast food or full service restaurant) and (2) the program director (or designated individual) of the respective regulatory authority. To provide the sufficient number of observations needed to conduct a statistically significant analysis of the data, FDA has determined that 400 data collections will be required in each of the two restaurant facility types. Therefore, the total number of responses will be 1,600 (400 data collections x 2 facility types x 2 respondents per data collection). The burden associated with the completion of Sections 1 and 3 of the form is specific to the persons in charge of the selected facilities. It includes the time it will take the person in charge to accompany the data collector during the site visit and answer the data collector's questions. The burden related to the completion of Section 2 of the form is specific to the program directors (or designated individuals) of the respective regulatory authorities. It includes the time it will take to answer the data collectors' questions and is the same regardless of the facility type. To calculate the estimate of the hours per response, FDA will use the average [[Page 5436]] data collection duration for the same facility types during the 2013- 2014 data collection. FDA estimates that it will take the persons in charge of full service restaurants and fast food restaurants 104 minutes (1.73 hours) and 82 minutes (1.36 hours), respectively, to accompany the data collectors while they complete Sections 1 and 3 of the form. In comparison, for the 2013-2014 data collection, the burden estimate was 106 minutes (1.76 hours) in full service restaurants and 73 minutes (1.21 hours) in fast food restaurants. FDA estimates that it will take the program director (or designated individual) of the respective regulatory authority 30 minutes (0.5 hours) to answer the questions related to Section 2 of the form. This burden estimate is unchanged from the last data collection. Hence, the total burden estimate for a data collection in a full service restaurant, including the responses of both the program director and the person in charge, is 134 minutes (104 + 30) (2.23 hours). The total burden estimate for a data collection in a fast food restaurant, including the responses of both the program director and the person in charge, is 112 minutes (82 + 30) (1.86 hours). Based on the number of entry refusals from the 2013-2014 baseline data collection, we estimate a refusal rate of 2 percent for the data collections within restaurant facility types. The estimate of the time per non-respondent is 5 minutes (0.08 hours) for the person in charge to listen to the purpose of the visit and provide a verbal refusal of entry. FDA estimates the burden of this collection of information as follows: Table 2--Estimated Annual Reporting Burden \1\ ------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------ Number of Number of Number of Total annual Number of non- responses per Total annual Activity respondents responses per responses respondents non- non- responses Average burden per response Total hours respondent respondent ------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------ 2021-2022 Data Collection (Fast Food 400 1 400 .............. .............. .............. 1.36................................ 544 Restaurants)--Completion of Sections 1 and 3. 2021-2022 Data Collection (Full Service 400 1 400 .............. .............. .............. 1.73................................ 692 Restaurants)--Completion of Sections 1 and 3. 2021-2022 Data Collection-Completion of 800 1 800 .............. .............. .............. 0.5 (30 minutes).................... 400 Section 2--All Facility Types. 2021-2022 Data Collection-Entry Refusals-- - - - 16 1 16 0.08 (5 minutes).................... 1.28 All Facility Types. ----------------------------------------------------------------------------------------------------------------------------------------------------- Total Hours............................... .............. .............. .............. .............. .............. .............. .................................... 1,637.28 ------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------ \1\ There are no capital costs or operating and maintenance costs associated with this collection of information. The burden for this information collection has not changed since the last OMB approval. II. References The following references are on display in the Dockets Management Staff (see ADDRESSES) and are available for viewing by interested persons between 9 a.m. and 4 p.m., Monday through Friday, they are also available electronically at https://www.regulations.gov. FDA has verified the website addresses, as of the date this document publishes in the Federal Register, but websites are subject to change over time. 1. ``Report of the FDA Retail Food Program Database of Foodborne Illness Risk Factors'' (2000). Available at: https://wayback.archive-it.org/7993/20170406023019/https://www.fda.gov/downloads/Food/GuidanceRegulation/UCM123546.pdf. 2. ``FDA Report on the Occurrence of Foodborne Illness Risk Factors in Selected Institutional Foodservice, Restaurant, and Retail Food Store Facility Types (2004).'' Available at: https://wayback.archive-it.org/7993/20170406023011/https://www.fda.gov/downloads/Food/GuidanceRegulation/RetailFoodProtection/FoodborneIllnessRiskFactorReduction/UCM423850.pdf. 3. ``FDA Report on the Occurrence of Foodborne Illness Risk Factors in Selected Institutional Foodservice, Restaurant, and Retail Food Store Facility Types (2009).'' Available at: https://wayback.archive-it.org/7993/20170406023004/https://www.fda.gov/Food/GuidanceRegulation/RetailFoodProtection/FoodborneIllnessRiskFactorReduction/ucm224321.htm. 4. FDA National Retail Food Team. ``FDA Trend Analysis Report on the Occurrence of Foodborne Illness Risk Factors in Selected Institutional Foodservice, Restaurant, and Retail Food Store Facility Types (1998-2008).'' Available at: https://wayback.archive-it.org/7993/20170406022950/https://www.fda.gov/Food/GuidanceRegulation/RetailFoodProtection/FoodborneIllnessRiskFactorReduction/ucm223293.htm. 5. ``FDA Food Code.'' Available at: https://www.fda.gov/FoodCode. Dated: January 31, 2018. Leslie Kux, Associate Commissioner for Policy. [FR Doc. 2018-02414 Filed 2-6-18; 8:45 am] BILLING CODE 4164-01-P
![Federal Register / Vol. 83, No. 26 / Wednesday, February 7, 2018 / Notices 5433
applicant. (See H. Rept. 857, part 1, 98th considered timely if they are information that you do not wish to be
Cong., 2d sess., pp. 41–42, 1984.) postmarked or the delivery service made publicly available, submit your
Petitions should be in the format acceptance receipt is on or before that comments only as a written/paper
specified in 21 CFR 10.30. date. submission. You should submit two
Submit petitions electronically to copies total. One copy will include the
Electronic Submissions information you claim to be confidential
https://www.regulations.gov at Docket
No. FDA–2013–S–0610. Submit written Submit electronic comments in the with a heading or cover note that states
petitions (two copies are required) to the following way: ‘‘THIS DOCUMENT CONTAINS
Dockets Management Staff (HFA–305), • Federal eRulemaking Portal: CONFIDENTIAL INFORMATION.’’ The
Food and Drug Administration, 5630 https://www.regulations.gov. Follow the Agency will review this copy, including
Fishers Lane, Rm. 1061, Rockville, MD instructions for submitting comments. the claimed confidential information, in
20852. Comments submitted electronically, its consideration of comments. The
including attachments, to https:// second copy, which will have the
Dated: January 31, 2018.
www.regulations.gov will be posted to claimed confidential information
Leslie Kux, the docket unchanged. Because your redacted/blacked out, will be available
Associate Commissioner for Policy. comment will be made public, you are for public viewing and posted on
[FR Doc. 2018–02403 Filed 2–6–18; 8:45 am] solely responsible for ensuring that your https://www.regulations.gov. Submit
BILLING CODE 4164–01–P comment does not include any both copies to the Dockets Management
confidential information that you or a Staff. If you do not wish your name and
third party may not wish to be posted, contact information to be made publicly
DEPARTMENT OF HEALTH AND such as medical information, your or available, you can provide this
HUMAN SERVICES anyone else’s Social Security number, or information on the cover sheet and not
confidential business information, such in the body of your comments and you
Food and Drug Administration
as a manufacturing process. Please note must identify this information as
[Docket No. FDA–2012–N–0547] that if you include your name, contact ‘‘confidential.’’ Any information marked
information, or other information that as ‘‘confidential’’ will not be disclosed
Agency Information Collection identifies you in the body of your except in accordance with 21 CFR 10.20
Activities; Proposed Collection; comments, that information will be and other applicable disclosure law. For
Comment Request; Survey on the posted on https://www.regulations.gov. more information about FDA’s posting
Occurrence of Foodborne Illness Risk • If you want to submit a comment of comments to public dockets, see 80
Factors in Selected Retail and with confidential information that you FR 56469, September 18, 2015, or access
Foodservice Facility Types do not wish to be made available to the the information at: https://www.gpo.gov/
AGENCY: Food and Drug Administration, public, submit the comment as a fdsys/pkg/FR-2015-09-18/pdf/2015-
HHS. written/paper submission and in the 23389.pdf.
manner detailed (see ‘‘Written/Paper Docket: For access to the docket to
ACTION: Notice. Submissions’’ and ‘‘Instructions’’). read background documents or the
SUMMARY: The Food and Drug Written/Paper Submissions electronic and written/paper comments
Administration (FDA or Agency) is received, go to https://
announcing an opportunity for public Submit written/paper submissions as www.regulations.gov and insert the
comment on the proposed collection of follows: docket number, found in brackets in the
• Mail/Hand delivery/Courier (for heading of this document, into the
certain information by the Agency.
written/paper submissions): Dockets ‘‘Search’’ box and follow the prompts
Under the Paperwork Reduction Act of
Management Staff (HFA–305), Food and and/or go to the Dockets Management
1995 (PRA), Federal Agencies are
Drug Administration, 5630 Fishers Staff, 5630 Fishers Lane, Rm. 1061,
required to publish notice in the
Lane, Rm. 1061, Rockville, MD 20852. Rockville, MD 20852.
Federal Register concerning each • For written/paper comments
proposed collection of information, FOR FURTHER INFORMATION CONTACT: Ila
submitted to the Dockets Management
including each proposed extension of an S. Mizrachi, Office of Operations, Food
Staff, FDA will post your comment, as
existing collection of information, and and Drug Administration, Three White
well as any attachments, except for
to allow 60 days for public comment in Flint North, 10A–12M, 11601
information submitted, marked and
response to the notice. This notice Landsdown St., North Bethesda, MD
identified, as confidential, if submitted
solicits comments on ‘‘Survey on the 20852, 301–796–7726, PRAStaff@
as detailed in ‘‘Instructions.’’
Occurrence of Foodborne Illness Risk Instructions: All submissions received fda.hhs.gov.
Factors in Selected Retail and must include the Docket No. FDA– SUPPLEMENTARY INFORMATION: Under the
Foodservice Facility Types.’’ 2012–N–0547 for ‘‘Survey on the PRA (44 U.S.C. 3501–3520), Federal
DATES: Submit either electronic or Occurrence of Foodborne Illness Risk Agencies must obtain approval from the
written comments on the collection of Factors in Selected Retail and Office of Management and Budget
information by April 9, 2018. Foodservice Facility Types.’’ Received (OMB) for each collection of
ADDRESSES: You may submit comments comments, those filed in a timely information they conduct or sponsor.
as follows. Please note that late, manner (see ADDRESSES), will be placed ‘‘Collection of information’’ is defined
untimely filed comments will not be in the docket and, except for those in 44 U.S.C. 3502(3) and 5 CFR
considered. Electronic comments must 1320.3(c) and includes Agency requests
sradovich on DSK3GMQ082PROD with NOTICES
submitted as ‘‘Confidential
be submitted on or before April 9, 2018. Submissions,’’ publicly viewable at or requirements that members of the
The https://www.regulations.gov https://www.regulations.gov or at the public submit reports, keep records, or
electronic filing system will accept Dockets Management Staff between 9 provide information to a third party.
comments until midnight Eastern Time a.m. and 4 p.m., Monday through Section 3506(c)(2)(A) of the PRA (44
at the end of April 9, 2018. Comments Friday. U.S.C. 3506(c)(2)(A)) requires Federal
received by mail/hand delivery/courier • Confidential Submissions—To Agencies to provide a 60-day notice in
(for written/paper submissions) will be submit a comment with confidential the Federal Register concerning each
VerDate Sep<11>2014 18:17 Feb 06, 2018 Jkt 244001 PO 00000 Frm 00034 Fmt 4703 Sfmt 4703 E:\FR\FM\07FEN1.SGM 07FEN1](https://thefederalregister.org/doc/83_FR_5459/page/1.svg)
![5436 Federal Register / Vol. 83, No. 26 / Wednesday, February 7, 2018 / Notices
data collection duration for the same designated individual) of the respective person in charge, is 112 minutes (82 +
facility types during the 2013–2014 data regulatory authority 30 minutes (0.5 30) (1.86 hours).
collection. FDA estimates that it will hours) to answer the questions related to Based on the number of entry refusals
take the persons in charge of full service Section 2 of the form. This burden from the 2013–2014 baseline data
restaurants and fast food restaurants 104 estimate is unchanged from the last data collection, we estimate a refusal rate of
minutes (1.73 hours) and 82 minutes collection. Hence, the total burden 2 percent for the data collections within
(1.36 hours), respectively, to accompany estimate for a data collection in a full restaurant facility types. The estimate of
the data collectors while they complete service restaurant, including the
Sections 1 and 3 of the form. In the time per non-respondent is 5
responses of both the program director minutes (0.08 hours) for the person in
comparison, for the 2013–2014 data
and the person in charge, is 134 minutes charge to listen to the purpose of the
collection, the burden estimate was 106
(104 + 30) (2.23 hours). The total burden visit and provide a verbal refusal of
minutes (1.76 hours) in full service
estimate for a data collection in a fast entry.
restaurants and 73 minutes (1.21 hours)
in fast food restaurants. FDA estimates food restaurant, including the responses FDA estimates the burden of this
that it will take the program director (or of both the program director and the collection of information as follows:
TABLE 2—ESTIMATED ANNUAL REPORTING BURDEN 1
Number of Number of
Total Number of Total Average
Number of responses responses
Activity annual non- annual non- burden per Total hours
respondents per per non-
responses respondents responses response
respondent respondent
2021–2022 Data 400 1 400 ........................ ........................ ........................ 1.36 ............................ 544
Collection (Fast
Food Res-
taurants)—Com-
pletion of Sec-
tions 1 and 3.
2021–2022 Data 400 1 400 ........................ ........................ ........................ 1.73 ............................ 692
Collection (Full
Service Res-
taurants)—Com-
pletion of Sec-
tions 1 and 3.
2021–2022 Data 800 1 800 ........................ ........................ ........................ 0.5 (30 minutes) ........ 400
Collection-Com-
pletion of Section
2—All Facility
Types.
2021–2022 Data ¥ ¥ ¥ 16 1 16 0.08 (5 minutes) ........ 1.28
Collection-Entry
Refusals—All Fa-
cility Types.
Total Hours .......... ........................ ........................ ........................ ........................ ........................ ........................ .................................... 1,637.28
1 There are no capital costs or operating and maintenance costs associated with this collection of information.
The burden for this information Retail Food Store Facility Types (2004).’’ Dated: January 31, 2018.
collection has not changed since the last Available at: https://wayback.archive-it.org/ Leslie Kux,
OMB approval. 7993/20170406023011/https://www.fda.gov/ Associate Commissioner for Policy.
downloads/Food/GuidanceRegulation/
II. References [FR Doc. 2018–02414 Filed 2–6–18; 8:45 am]
RetailFoodProtection/FoodborneIllness
RiskFactorReduction/UCM423850.pdf. BILLING CODE 4164–01–P
The following references are on 3. ‘‘FDA Report on the Occurrence of
display in the Dockets Management Foodborne Illness Risk Factors in Selected
Staff (see ADDRESSES) and are available Institutional Foodservice, Restaurant, and DEPARTMENT OF HEALTH AND
for viewing by interested persons Retail Food Store Facility Types (2009).’’ HUMAN SERVICES
between 9 a.m. and 4 p.m., Monday Available at: https://wayback.archive-it.org/
through Friday, they are also available 7993/20170406023004/https://www.fda.gov/ Food and Drug Administration
electronically at https:// Food/GuidanceRegulation/RetailFood
Protection/FoodborneIllnessRiskFactor [Docket Nos. FDA–2015–E–0857 and FDA–
www.regulations.gov. FDA has verified 2015–E–0858]
Reduction/ucm224321.htm.
the website addresses, as of the date this
4. FDA National Retail Food Team. ‘‘FDA
document publishes in the Federal Trend Analysis Report on the Occurrence of
Determination of Regulatory Review
Register, but websites are subject to Foodborne Illness Risk Factors in Selected Period for Purposes of Patent
change over time. Institutional Foodservice, Restaurant, and Extension; FARXIGA
1. ‘‘Report of the FDA Retail Food Program Retail Food Store Facility Types (1998–
sradovich on DSK3GMQ082PROD with NOTICES
AGENCY: Food and Drug Administration,
Database of Foodborne Illness Risk Factors’’ 2008).’’ Available at: https://
wayback.archive-it.org/7993/201704
HHS.
(2000). Available at: https://wayback.archive-
it.org/7993/20170406023019/https:// 06022950/https://www.fda.gov/Food/ ACTION: Notice.
www.fda.gov/downloads/Food/Guidance GuidanceRegulation/RetailFoodProtection/
Regulation/UCM123546.pdf. FoodborneIllnessRiskFactorReduction/ SUMMARY: The Food and Drug
2. ‘‘FDA Report on the Occurrence of ucm223293.htm. Administration (FDA or the Agency) has
Foodborne Illness Risk Factors in Selected 5. ‘‘FDA Food Code.’’ Available at: https:// determined the regulatory review period
Institutional Foodservice, Restaurant, and www.fda.gov/FoodCode. for FARXIGA and is publishing this
VerDate Sep<11>2014 18:17 Feb 06, 2018 Jkt 244001 PO 00000 Frm 00037 Fmt 4703 Sfmt 4703 E:\FR\FM\07FEN1.SGM 07FEN1](https://thefederalregister.org/doc/83_FR_5459/page/4.svg)
Document Created: 2018-10-26 13:55:33
Document Modified: 2018-10-26 13:55:33
| Category | Regulatory Information | |
| Collection | Federal Register | |
| sudoc Class | AE 2.7: GS 4.107: AE 2.106: | |
| Publisher | Office of the Federal Register, National Archives and Records Administration | |
| Section | Notices | |
| Action | Notice. | |
| Dates | Submit either electronic or written comments on the collection of information by April 9, 2018. | |
| Contact | Ila S. Mizrachi, Office of Operations, Food and Drug Administration, Three White Flint North, 10A-12M, 11601 Landsdown St., North Bethesda, MD 20852, 301-796-7726, [email protected] | |
| FR Citation | 83 FR 5433 |
2025 Federal Register | Disclaimer | Privacy Policy
USC | CFR | eCFR