82 FR 13506 - Bulk Manufacturer of Controlled Substances Application: Siemens Healthcare Diagnostics, Inc.

DEPARTMENT OF JUSTICE
Drug Enforcement Administration

Federal Register Volume 82, Issue 47 (March 13, 2017)

Page Range		13506-13506
FR Document		2017-04875

Federal Register, Volume 82 Issue 47 (Monday, March 13, 2017)

[Federal Register Volume 82, Number 47 (Monday, March 13, 2017)]
[Notices]
[Page 13506]
From the Federal Register Online  [www.thefederalregister.org]
[FR Doc No: 2017-04875]


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DEPARTMENT OF JUSTICE

Drug Enforcement Administration

[Docket No. DEA-392]


Bulk Manufacturer of Controlled Substances Application: Siemens 
Healthcare Diagnostics, Inc.

ACTION: Notice of application.

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DATES: Registered bulk manufacturers of the affected basic classes, and 
applicants therefore, may file written comments on or objections to the 
issuance of the proposed registration in accordance with 21 CFR 
1301.33(a) on or before May 12, 2017.

ADDRESSES: Written comments should be sent to: Drug Enforcement 
Administration, Attention: DEA Federal Register Representative/DRW, 
8701 Morrissette Drive, Springfield, Virginia 22152.

SUPPLEMENTARY INFORMATION: The Attorney General has delegated his 
authority under the Controlled Substances Act to the Administrator of 
the Drug Enforcement Administration (DEA), 28 CFR 0.100(b). Authority 
to exercise all necessary functions with respect to the promulgation 
and implementation of 21 CFR part 1301, incident to the registration of 
manufacturers, distributors, dispensers, importers, and exporters of 
controlled substances (other than final orders in connection with 
suspension, denial, or revocation of registration) has been redelegated 
to the Assistant Administrator of the DEA Diversion Control Division 
(``Assistant Administrator'') pursuant to section 7 of 28 CFR part 0, 
appendix to subpart R.
    In accordance with 21 CFR 1301.33(a), this is notice that on 
December 14, 2016, Siemens Healthcare Diagnostics, Inc., Attn: RA, 100 
GBC Drive, Mailstop 514, Newark, Delaware 19702 applied to be 
registered as a bulk manufacturer of Ecgonine (9180) a basic class of 
controlled substance listed in schedule II.
    The company plans to produce the listed controlled substance in 
bulk to be used in the manufacture of DEA exempt products.

    Dated: March 6, 2017.
Louis J. Milione,
Assistant Administrator.
[FR Doc. 2017-04875 Filed 3-10-17; 8:45 am]
 BILLING CODE 4410-09-P

13506 Federal Register / Vol. 82, No. 47 / Monday, March 13, 2017 / Notices

Issued: March 7, 2017. Dated: March 6, 2017. —Minimize the burden of the collection
Lisa R. Barton, Louis J. Milione, of information on those who are to
Secretary to the Commission. Assistant Administrator. respond, including through the use of
[FR Doc. 2017–04790 Filed 3–10–17; 8:45 am] [FR Doc. 2017–04875 Filed 3–10–17; 8:45 am] appropriate automated, electronic,
BILLING CODE 7020–02–P BILLING CODE 4410–09–P mechanical, or other technological
collection techniques or other forms
of information technology, e.g.,
DEPARTMENT OF JUSTICE permitting electronic submission of
DEPARTMENT OF JUSTICE responses.
Federal Bureau of Investigation
Overview of This Information
Drug Enforcement Administration [OMB Number 1110–0058] Collection
Agency Information Collection 1. Type of Information Collection:
[Docket No. DEA–392]
Activities; Proposed eCollection Extension, with change of a currently
Bulk Manufacturer of Controlled eComments Requested; Extension approved collection.
Substances Application: Siemens With Change, of a Currently Approved 2. The Title of the Form/Collection:
Healthcare Diagnostics, Inc. Collection; National Incident-Based National Incident-Based Reporting
Reporting System (NIBRS) System.
3. The agency form number, if any,
ACTION: Notice of application. AGENCY: Federal Bureau of and the applicable component of the
Investigation, Department of Justice. Department sponsoring the collection:
DATES: Registered bulk manufacturers of ACTION: 60-Day notice. The form number is 1110–0058. The
the affected basic classes, and applicable component within the
applicants therefore, may file written SUMMARY: The Department of Justice Department of Justice is the Criminal
comments on or objections to the (DOJ), Federal Bureau of Investigation Justice Information Services Division, in
issuance of the proposed registration in (FBI), Criminal Justice Information the Federal Bureau of Investigation.
accordance with 21 CFR 1301.33(a) on Services Division (CJIS), will be 4. Affected public who will be asked
or before May 12, 2017. submitting the following information or required to respond, as well as a brief
collection request to the Office of abstract:
ADDRESSES: Written comments should Management and Budget (OMB) for Primary: City, county, state, tribal and
be sent to: Drug Enforcement review and approval in accordance with federal law enforcement agencies.
Administration, Attention: DEA Federal the Paperwork Reduction Act of 1995. Abstract: Under U.S. Code, Title 28,
Register Representative/DRW, 8701 DATES: Comments are encouraged and Section 534, Acquisition, Preservation,
Morrissette Drive, Springfield, Virginia will be accepted for 60 days until May and Exchange of Identification Records;
22152. 12, 2017. Appointment of Officials, June 11, 1930;
SUPPLEMENTARY INFORMATION: The FOR FURTHER INFORMATION CONTACT: All Public Law 109–177 (H.R. 3199), March
Attorney General has delegated his comments, suggestions, or questions 9, 2006, USA Patriot Improvement and
authority under the Controlled regarding additional information, to Reauthorization Act of 2005; Public Law
Substances Act to the Administrator of include obtaining a copy of the 110–457, Title II, Section 237(a), (b),
the Drug Enforcement Administration proposed information collection December 23, 2008, the William
(DEA), 28 CFR 0.100(b). Authority to instrument with instructions, should be Wilberforce Trafficking Victims
exercise all necessary functions with directed to Mrs. Amy C. Blasher, Unit Reauthorization Act of 2008, and
respect to the promulgation and Chief, Federal Bureau of Investigation, Matthew Shepard Hate Crimes
implementation of 21 CFR part 1301, Criminal Information Services Division, Prevention Act, April 28, 2009, this
incident to the registration of Module E–3, 1000 Custer Hollow Road, collection requests Incident data from
manufacturers, distributors, dispensers, Clarksburg, West Virginia 26306; city, county, state, tribal and federal law
importers, and exporters of controlled facsimile (304) 625–3566. enforcement agencies in order for the
substances (other than final orders in SUPPLEMENTARY INFORMATION: Written FBI UCR Program to serve as the
connection with suspension, denial, or comments and suggestions from the national clearinghouse for the collection
revocation of registration) has been public and affected agencies concerning and dissemination of incident data and
redelegated to the Assistant the proposed collection of information to publish these statistics in Crime in
Administrator of the DEA Diversion are encouraged. Your comments should the United States, Hate Crime Statistics,
Control Division (‘‘Assistant address one or more of the following and Law Enforcement Officers Killed
Administrator’’) pursuant to section 7 of four points: and Assaulted. NIBRS is an incident-
28 CFR part 0, appendix to subpart R. —Evaluate whether the proposed based reporting system in which law
collection of information is necessary enforcement collects data on each crime
In accordance with 21 CFR occurrence. Designed to be generated as
1301.33(a), this is notice that on for the proper performance of the
functions of the Federal Bureau of a byproduct of local, state, and federal
December 14, 2016, Siemens Healthcare automated records systems, currently,
Investigation, including whether the
Diagnostics, Inc., Attn: RA, 100 GBC the NIBRS collects data on each
information will have practical utility;
Drive, Mailstop 514, Newark, Delaware —Evaluate the accuracy of the agency’s incident and arrest within 24 crime
19702 applied to be registered as a bulk categories made up of 52 specific crimes
mstockstill on DSK3G9T082PROD with NOTICES

estimate of the burden of the
manufacturer of Ecgonine (9180) a basic proposed collection of information, called Group A offenses. For each of the
class of controlled substance listed in including the validity of the offenses coming to the attention of law
schedule II. methodology and assumptions used; enforcement, various facts about the
The company plans to produce the —Evaluate whether and if so how the crime are collected. In addition to the
listed controlled substance in bulk to be quality, utility, and clarity of the Group A offenses, there are 10 Group B
used in the manufacture of DEA exempt information to be collected can be offense categories for which only arrest
products. enhanced; and data are reported. The most significant

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Document Created: 2018-02-01 14:57:53
Document Modified: 2018-02-01 14:57:53

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 application.
Dates		Registered bulk manufacturers of the affected basic classes, and applicants therefore, may file written comments on or objections to the issuance of the proposed registration in accordance with 21 CFR 1301.33(a) on or before May 12, 2017.
FR Citation		82 FR 13506

82 FR 13506 - Bulk Manufacturer of Controlled Substances Application: Siemens Healthcare Diagnostics, Inc.

DEPARTMENT OF JUSTICEDrug Enforcement Administration

Federal Register Volume 82, Issue 47 (March 13, 2017)

DEPARTMENT OF JUSTICE
Drug Enforcement Administration