81 FR 39052 - Information Collection; Report of Shipment

DEPARTMENT OF DEFENSE
GENERAL SERVICES ADMINISTRATION
NATIONAL AERONAUTICS AND SPACE ADMINISTRATION

Federal Register Volume 81, Issue 115 (June 15, 2016)

Page Range		39052-39053
FR Document		2016-14119

Under the provisions of the Paperwork Reduction Act, the Regulatory Secretariat Division will be submitting to the Office of Management and Budget (OMB) a request to review and approve an extension of a previously approved information collection requirement concerning report of shipment.

Federal Register, Volume 81 Issue 115 (Wednesday, June 15, 2016)

[Federal Register Volume 81, Number 115 (Wednesday, June 15, 2016)]
[Notices]
[Pages 39052-39053]
From the Federal Register Online  [www.thefederalregister.org]
[FR Doc No: 2016-14119]


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DEPARTMENT OF DEFENSE

GENERAL SERVICES ADMINISTRATION

NATIONAL AERONAUTICS AND SPACE ADMINISTRATION

[OMB Control No. 9000-0056; Docket 2016-0053; Sequence 23]


Information Collection; Report of Shipment

AGENCY: Department of Defense (DOD), General Services Administration 
(GSA), and National Aeronautics and Space Administration (NASA).

ACTION: Notice of request for public comments regarding an extension of 
an existing OMB clearance.

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SUMMARY: Under the provisions of the Paperwork Reduction Act, the 
Regulatory Secretariat Division will be submitting to the Office of 
Management and Budget (OMB) a request to review and approve an 
extension of a previously approved information collection requirement 
concerning report of shipment.

DATES: Submit comments on or before August 15, 2016.

ADDRESSES: Submit comments identified by Information Collection 9000-
0056, Report of Shipment, by any of the following methods:
     Regulations.gov: http://www.regulations.gov.
    Submit comments via the Federal eRulemaking portal by searching the 
OMB control number. Select the link ``Submit a Comment'' that 
corresponds with ``Information Collection 9000-0056, Report of 
Shipment''. Follow the instructions provided at the ``Submit a 
Comment'' screen. Please include your name, company name (if any), and 
``Information Collection 9000-0056, Report of Shipment'' on your 
attached document.
     Mail: General Services Administration, Regulatory 
Secretariat Division (MVCB), 1800 F Street NW., Washington, DC 20405. 
ATTN: Ms. Flowers/IC 9000-0056, Report of Shipment.
    Instructions: Please submit comments only and cite Information 
Collection 9000-0056, Report of Shipment, in all correspondence related 
to this collection. Comments received generally will be posted without 
change to http://www.regulations.gov, including any personal and/or 
business confidential information provided. To confirm receipt of your 
comment(s), please check www.regulations.gov, approximately two to 
three days after submission to verify posting (except allow 30 days for 
posting of comments submitted by mail).

FOR FURTHER INFORMATION CONTACT: Mr. Curtis E. Glover, Sr., Procurement 
Analyst, Office of Acquisition Policy, by telephone at 202-501-1448 or 
curtis.glover@gsa.gov.

SUPPLEMENTARY INFORMATION: 

A. Purpose

    Per FAR 47.208, military (and, as required, civilian agency) 
storage and distribution points, depots, and other receiving activities 
require advance notice of shipments en-route from contractors' plants. 
Generally, this notification is required only for classified material; 
sensitive, controlled, and certain other protected material; 
explosives, and some other hazardous materials; selected shipments 
requiring movement control; or minimum carload or truckload shipments. 
It facilitates arrangements for transportation control, labor, space, 
and use of materials handling equipment at destination. Also, timely 
receipt of notices by the consignee transportation office precludes the 
incurring of demurrage and vehicle detention charges. Unless otherwise 
directed by a contracting officer, a contractor shall send the notice 
to the consignee transportation office at least twenty-four hours 
before the arrival of the shipment.

B. Annual Reporting Burden

    Respondents: 33.
    Responses per Respondent: 303.
    Annual Responses: 9,999.
    Hours per Response: .167.
    Total Burden Hours: 1,670.

C. Public Comments

    Public comments are particularly invited on: Whether this 
collection of information is necessary; whether it will have practical 
utility; whether our estimate of the public burden of this collection 
of information is accurate, and based on valid assumptions and 
methodology; ways to enhance the quality, utility, and clarity of the 
information to be collected; and ways in which we can minimize the 
burden of the collection of information on those who are to respond, 
through the use of appropriate technological collection techniques or 
other forms of information technology.

[[Page 39053]]

    Obtaining Copies of Proposals: Requesters may obtain a copy of the 
information collection documents from the General Services 
Administration, Regulatory Secretariat Division (MVCB), 1800 F Street, 
Washington, DC 20405, telephone 202-501-4755. Please cite OMB Control 
No. 9000-0056, Report of Shipment, in all correspondence.

    Dated: June 9, 2016.
Lorin S. Curit,
Director, Federal Acquisition Policy Division, Office of Governmentwide 
Acquisition Policy, Office of Acquisition Policy, Office of 
Governmentwide Policy.
[FR Doc. 2016-14119 Filed 6-14-16; 8:45 am]
 BILLING CODE 6820-EP-P

Federal Register / Vol. 81, No. 115 / Wednesday, June 15, 2016 / Notices 39053

Obtaining Copies of Proposals: Hampshire Ave., Silver Spring, MD and flavors) (see 81 FR 28973, May 10,
Requesters may obtain a copy of the 20993–0002, 877–287–1373, email: 2016),
information collection documents from CTPRegulations@fda.hhs.gov. • Laboratory facilities that perform
the General Services Administration, SUPPLEMENTARY INFORMATION: tobacco testing (whether third-party or
Regulatory Secretariat Division (MVCB), in-house), and
1800 F Street, Washington, DC 20405, I. Background • Manufacturing facilities for tobacco
telephone 202–501–4755. Please cite On June 22, 2009, the Family products for further manufacturing into
OMB Control No. 9000–0056, Report of Smoking Prevention and Tobacco finished tobacco products (including,
Shipment, in all correspondence. Control Act (Pub. L. 111–31; 123 Stat. but not limited to, components, parts,
1776) was signed into law, amending flavors, casings, e-liquids).
Dated: June 9, 2016. Please note that Tobacco Product
the Federal Food, Drug, and Cosmetic
Lorin S. Curit, Manufacturing Facility Visits are not
Act (the FD&C Act) and giving FDA
Director, Federal Acquisition Policy Division, authority to regulate tobacco product intended to include or replace official
Office of Governmentwide Acquisition Policy, FDA inspections of facilities to
manufacturing, distribution, and
Office of Acquisition Policy, Office of determine compliance with the FD&C
Governmentwide Policy. marketing. The new provisions include,
among other things, the authority to Act; rather, these facility visits are
[FR Doc. 2016–14119 Filed 6–14–16; 8:45 am] meant to educate FDA staff and improve
issue regulations related to tobacco
BILLING CODE 6820–EP–P
product manufacturing practice in order their understanding of the tobacco
to protect the public health and to industry and its manufacturing
assure that tobacco products are in operations.
DEPARTMENT OF HEALTH AND compliance with the FD&C Act.
HUMAN SERVICES III. Site Selection
Specifically, section 906(e) of the FD&C
Act (21 U.S.C. 387f(e)) provides that in CTP plans to select sites from one or
Food and Drug Administration more of each of the following categories:
applying manufacturing restrictions to
• Dissolvable products,
[Docket No. FDA–2012–N–0853] tobacco, the Secretary shall prescribe • Gels,
regulations (which may differ based on • Cigars,
Tobacco Product Manufacturing the type of tobacco product involved) • Pipe tobacco,
Facility Visits requiring that the methods used in, and • Waterpipe tobacco products,
AGENCY: Food and Drug Administration, the facilities and controls used for, the • ENDS (including e-cigarettes, e-
HHS. manufacture, preproduction design hookah, e-cigars, vape pens, advanced
ACTION: Notice. validation (including a process to assess refillable personal vaporizers, and
the performance of a tobacco product), electronic pipes) and liquid nicotine
SUMMARY: The Food and Drug packing, and storage of a tobacco and flavors,
Administration (FDA), Center for product conform to current good • Tobacco laboratories,
Tobacco Products (CTP) is announcing manufacturing practice, or hazard • Importers of finished tobacco
an invitation for participation in its analysis and critical control point products,
Tobacco Product Manufacturing Facility methodology. • Distributors and wholesalers of
Visits. This program is intended to give CTP is instituting Tobacco Product regulated tobacco products, and/or
FDA staff an opportunity to visit Manufacturing Facility Visits to provide • Manufacturers of tobacco products
facilities involved in the manufacturing FDA staff with the opportunity to: for further manufacturing into finished
of newly deemed tobacco products and • Observe tobacco product tobacco products (including, but not
their components and parts, including manufacturing operations—from the limited to, components, parts, flavors,
any related laboratory testing, and to receipt of raw materials to the casings, e-liquids).
observe the manufacturing operations of distribution of newly deemed tobacco Final site selections will be based on
the tobacco industry. The purpose of products, and the availability of CTP funds and
this document is to invite parties • Learn about the manufacturing resources for the relevant fiscal year, as
interested in participating in Tobacco practices and processes unique to your well as the following factors, as
Product Manufacturing Facility Visits to facility and newly deemed tobacco applicable: (1) Compliance status of the
submit requests to CTP. products. requesting facility and affiliated firm; (2)
This program will also inform FDA whether the requesting facility or
DATES: Submit either an electronic or
staff as they implement the tobacco affiliated firm, if applicable, has a
written request for participation by
provisions of the FD&C Act. significant request or marketing
August 15, 2016. See section IV of this
application or submission pending with
document for information on requests II. Description of the Tobacco Product
FDA; and (3) whether the requesting
for participation. Manufacturing Facility Visits
facility will be engaged in active
ADDRESSES: If your facility is interested In this program, groups of FDA staff manufacturing or processing during the
in participating in Tobacco Product plan to observe the following facilities proposed time of the visit. All travel
Manufacturing Facility Visits, please and their operations: expenses associated with Tobacco
submit a request either electronically to • Manufacturing facilities, including Product Manufacturer Facility Visits
http://www.regulations.gov or in writing establishments that process, package, will be the responsibility of CTP.
to the Division of Dockets Management label, and distribute different types of
(HFA–305), Food and Drug newly deemed tobacco products (e.g., IV. Requests for Participation
Administration, 5630 Fishers Lane, Rm.
ehiers on DSK5VPTVN1PROD with NOTICES

dissolvable products, gels, cigars, pipe The request for participation should
1061, Rockville, MD 20852. tobacco, waterpipe tobacco products, include the following identification
FOR FURTHER INFORMATION CONTACT: and electronic nicotine delivery systems information:
Matthew Brenner, Center for Tobacco (ENDS) (including e-cigarettes, e- • The name and contact information
Products, Food and Drug hookah, e-cigars, vape pens, advanced (including address, phone number, and
Administration, Document Control refillable personal vaporizers, and email) of your point of contact for the
Center, Bldg. 71, Rm. G335, 10903 New electronic pipes) and liquid nicotine request;

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Document Created: 2016-06-15 02:21:12
Document Modified: 2016-06-15 02:21:12

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 of request for public comments regarding an extension of an existing OMB clearance.
Dates		Submit comments on or before August 15, 2016.
Contact		Mr. Curtis E. Glover, Sr., Procurement Analyst, Office of Acquisition Policy, by telephone at 202-501-1448 or [email protected]
FR Citation		81 FR 39052

81 FR 39052 - Information Collection; Report of Shipment

DEPARTMENT OF DEFENSEGENERAL SERVICES ADMINISTRATIONNATIONAL AERONAUTICS AND SPACE ADMINISTRATION

Federal Register Volume 81, Issue 115 (June 15, 2016)

DEPARTMENT OF DEFENSE
GENERAL SERVICES ADMINISTRATION
NATIONAL AERONAUTICS AND SPACE ADMINISTRATION