Agency Information Collection Activities; Proposed eCollection eComments Requested; Registrant Record of Controlled Substances Destroyed, 99-100 [2023-28816]
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khammond on DSKJM1Z7X2PROD with NOTICES
Federal Register / Vol. 89, No. 1 / Tuesday, January 2, 2024 / Notices
including antidumping or
countervailing duties). If you are a
trade/business association, provide the
information, on an aggregate basis, for
the firms which are members of your
association.
(a) Production (quantity) and, if
known, an estimate of the percentage of
total production of Subject Merchandise
in the Subject Country accounted for by
your firm’s(s’) production;
(b) Capacity (quantity) of your firm(s)
to produce the Subject Merchandise in
the Subject Country (that is, the level of
production that your establishment(s)
could reasonably have expected to
attain during the year, assuming normal
operating conditions (using equipment
and machinery in place and ready to
operate), normal operating levels (hours
per week/weeks per year), time for
downtime, maintenance, repair, and
cleanup, and a typical or representative
product mix); and
(c) the quantity and value of your
firm’s(s’) exports to the United States of
Subject Merchandise and, if known, an
estimate of the percentage of total
exports to the United States of Subject
Merchandise from the Subject Country
accounted for by your firm’s(s’) exports.
(12) Identify significant changes, if
any, in the supply and demand
conditions or business cycle for the
Domestic Like Product that have
occurred in the United States or in the
market for the Subject Merchandise in
the Subject Country since the Order
Dates, and significant changes, if any,
that are likely to occur within a
reasonably foreseeable time. Supply
conditions to consider include
technology; production methods;
development efforts; ability to increase
production (including the shift of
production facilities used for other
products and the use, cost, or
availability of major inputs into
production); and factors related to the
ability to shift supply among different
national markets (including barriers to
importation in foreign markets or
changes in market demand abroad).
Demand conditions to consider include
end uses and applications; the existence
and availability of substitute products;
and the level of competition among the
Domestic Like Product produced in the
United States, Subject Merchandise
produced in the Subject Country, and
such merchandise from other countries.
(13) (OPTIONAL) A statement of
whether you agree with the above
definitions of the Domestic Like Product
and Domestic Industry; if you disagree
with either or both of these definitions,
please explain why and provide
alternative definitions.
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Authority: This proceeding is being
conducted under authority of Title VII
of the Tariff Act of 1930; this notice is
published pursuant to § 207.61 of the
Commission’s rules.
By order of the Commission.
Issued: December 21, 2023.
Lisa Barton,
Secretary to the Commission.
[FR Doc. 2023–28536 Filed 12–29–23; 8:45 am]
BILLING CODE 7020–02–P
JUDICIAL CONFERENCE OF THE
UNITED STATES
Advisory Committee on Appellate
Rules; Hearing of the Judicial
Conference
Judicial Conference of the
United States.
ACTION: Advisory Committee on
Appellate Rules; notice of cancellation
of open hearing.
AGENCY:
The following public hearing
on proposed amendments to the Federal
Rules of Appellate Procedure has been
canceled: Appellate Rules Hearing on
January 24, 2024.
DATES: January 24, 2024.
FOR FURTHER INFORMATION CONTACT: H.
Thomas Byron III, Esq., Chief Counsel,
Rules Committee Staff, Administrative
Office of the U.S. Courts, Thurgood
Marshall Federal Judiciary Building,
One Columbus Circle NE, Suite 7–300,
Washington, DC 20544, Phone (202)
502–1820, RulesCommittee_Secretary@
ao.uscourts.gov.
SUPPLEMENTARY INFORMATION: The
announcement for this hearing was
previously published in the Federal
Register on August 9, 2023 at 88 FR
53917.
SUMMARY:
(Authority: 28 U.S.C. 2073.)
Dated: December 27, 2023.
Shelly L. Cox,
Management Analyst, Rules Committee Staff.
[FR Doc. 2023–28826 Filed 12–29–23; 8:45 am]
BILLING CODE 2210–55–P
DEPARTMENT OF JUSTICE
[OMB Number 1117–0007]
Agency Information Collection
Activities; Proposed eCollection
eComments Requested; Registrant
Record of Controlled Substances
Destroyed
Drug Enforcement
Administration, Department of Justice.
ACTION: 30-Day notice.
AGENCY:
PO 00000
Frm 00057
Fmt 4703
Sfmt 4703
99
The Drug Enforcement
Administration, Department of Justice
(DOJ), will be submitting the following
information collection request to the
Office of Management and Budget
(OMB) for review and approval in
accordance with the Paperwork
Reduction Act of 1995. This proposed
information collection was previously
published in the Federal Register on
October 26, 2023, allowing for a 60-day
comment period.
DATES: Comments are encouraged and
will be accepted for 30 days until
February 1, 2023.
FOR FURTHER INFORMATION CONTACT: If
you have comments especially on the
estimated public burden or associated
response time, suggestions, or need a
copy of the proposed information
collection instrument with instructions
or additional information, please
contact Scott A. Brinks, Regulatory
Drafting and Policy Support Section,
Drug Enforcement Administration;
Mailing Address: 8701 Morrissette
Drive, Springfield, Virginia 22152;
Telephone: (571) 362–3261; email:
DPW@dea.gov.
SUPPLEMENTARY INFORMATION: Written
comments and suggestions from the
public and affected agencies concerning
the proposed collection of information
are encouraged. Your comments should
address one or more of the following
four points:
—Evaluate whether the proposed
collection of information is necessary
for the proper performance of the
functions of the agency, including
whether the information will have
practical utility;
—Evaluate the accuracy of the agency’s
estimate of the burden of the
proposed collection of information,
including the validity of the
methodology and assumptions used;
—Enhance the quality, utility, and
clarity of the information to be
collected; and/or
—Minimize the burden of the collection
of information on those who are to
respond, including through the use of
appropriate automated, electronic,
mechanical, or other technological
collection techniques or other forms
of information technology, e.g.,
permitting electronic submission of
responses.
SUMMARY:
Written comments and
recommendations for this information
collection should be submitted within
30 days of the publication of this notice
on the following website
www.reginfo.gov/public/do/PRAMain.
Find this particular information
collection by selecting ‘‘Currently under
E:\FR\FM\02JAN1.SGM
02JAN1
100
Federal Register / Vol. 89, No. 1 / Tuesday, January 2, 2024 / Notices
khammond on DSKJM1Z7X2PROD with NOTICES
30-day Review—Open for Public
Comments’’ or by using the search
function and entering either the title of
the information collection or the OMB
Control Number 1117–0007. This
information collection request may be
viewed at www.reginfo.gov. Follow the
instructions to view Department of
Justice, information collections
currently under review by OMB.
DOJ seeks PRA authorization for this
information collection for three (3)
years. OMB authorization for an ICR
cannot be for more than three (3) years
without renewal. The DOJ notes that
information collection requirements
submitted to the OMB for existing ICRs
receive a month-to-month extension
while they undergo review.
Overview of This Information
Collection
1. Type of Information Collection:
Extension of a currently approved
collection.
2. Title of the Form/Collection:
Registrant Record of Controlled
Substances Destroyed.
3. Agency form number, if any, and
the applicable component of the
Department of Justice sponsoring the
collection: DEA From 41. The
applicable component within the
Department of Justice is the Drug
Enforcement Administration, Diversion
Control Division.
4. Affected public who will be asked
or required to respond, as well as a brief
abstract:
Affected public (Primary): Private
Sector—business or other for-profit.
Affected public (Other): Not-for-profit
institutions; Federal, State, local, and
tribal governments.
Abstract: In accordance with the
Controlled Substance Act (CSA), every
DEA registrant must make a biennial
inventory and maintain, on a current
basis, a complete and accurate record of
each controlled substance
manufactured, received, sold, delivered,
or otherwise disposed of. 21 U.S.C. 827
and 958. These records must be
maintained separately from all other
records of the registrant or,
alternatively, in the case of non-narcotic
controlled substances, be in such form
that required information is readily
retrievable from the ordinary business
records of the registrant per 21 U.S.C.
827(b)(2). The records must be kept and
be available for at least two years for
inspection and copying by officers or
employees of the United States
authorized by the Attorney General. 21
U.S.C. 827(b)(3). The records must be in
accordance with and contain such
relevant information as may be required
by regulations promulgated by DEA. 21
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15:59 Dec 29, 2023
Jkt 262001
U.S.C. 827(b)(1). These record
requirements help to deter and detect
diversion of controlled substances and
ensure that registrants remain
accountable for all controlled
substances within their possession and/
or control.
5. Obligation to Respond: Mandatory
per 21 CFR 1314.
6. Total Estimated Number of
Respondents: 92,832.
7. Estimated Time per Respondent: 30
minutes for DEA Form 41.
8. Frequency: DEA Form 41 is 1 per
year.
9. Total Estimated Annual Time
Burden: 46,416 hours.
10. Total Estimated Annual Other
Costs Burden: $0.
If additional information is required,
contact: Darwin Arceo, Department
Clearance Officer, Policy and Planning
Staff, Justice Management Division,
United States Department of Justice,
Two Constitution Square, 145 N Street
NE, 4W–218, Washington, DC 20530.
Dated: December 27, 2023.
Darwin Arceo,
Department Clearance Officer for PRA, U.S.
Department of Justice.
[FR Doc. 2023–28816 Filed 12–29–23; 8:45 am]
BILLING CODE 4410–09–P
DEPARTMENT OF JUSTICE
[OMB Number 1117–0046]
Agency Information Collection
Activities; Proposed eCollection
eComments Requested; SelfCertification, Training, and Logbooks
for Regulated Sellers and Mail-Order
Distributors of Scheduled Listed
Chemicals Products
Drug Enforcement
Administration, Department of Justice.
ACTION: 30-Day notice.
AGENCY:
The Drug Enforcement
Administration (DEA), Department of
Justice (DOJ), will be submitting the
following information collection request
to the Office of Management and Budget
(OMB) for review and approval in
accordance with the Paperwork
Reduction Act of 1995. This proposed
information collection was previously
published in the Federal Register on
October 26, 2023, allowing for a 60-day
comment period.
DATES: Comments are encouraged and
will be accepted for 30 days until
February 1, 2023.
FOR FURTHER INFORMATION CONTACT: If
you have comments especially on the
estimated public burden or associated
response time, suggestions, or need a
SUMMARY:
PO 00000
Frm 00058
Fmt 4703
Sfmt 4703
copy of the proposed information
collection instrument with instructions
or additional information, please
contact Scott A. Brinks, Regulatory
Drafting and Policy Support Section,
Drug Enforcement Administration;
Mailing Address: 8701 Morrissette
Drive, Springfield, Virginia 22152;
Telephone: (571) 362–3261, email:
DPW@dea.gov.
SUPPLEMENTARY INFORMATION: Written
comments and suggestions from the
public and affected agencies concerning
the proposed collection of information
are encouraged. Your comments should
address one or more of the following
four points:
—Evaluate whether the proposed
collection of information is necessary
for the proper performance of the
functions of the agency, including
whether the information will have
practical utility;
—Evaluate the accuracy of the agency’s
estimate of the burden of the
proposed collection of information,
including the validity of the
methodology and assumptions used;
—Enhance the quality, utility, and
clarity of the information to be
collected; and/or
—Minimize the burden of the collection
of information on those who are to
respond, including through the use of
appropriate automated, electronic,
mechanical, or other technological
collection techniques or other forms
of information technology, e.g.,
permitting electronic submission of
responses.
Written comments and
recommendations for this information
collection should be submitted within
30 days of the publication of this notice
on the following website
www.reginfo.gov/public/do/PRAMain.
Find this particular information
collection by selecting ‘‘Currently under
30-day Review—Open for Public
Comments’’ or by using the search
function and entering either the title of
the information collection or the OMB
Control Number 1117–0046. This
information collection request may be
viewed at www.reginfo.gov. Follow the
instructions to view Department of
Justice, information collections
currently under review by OMB.
DOJ seeks PRA authorization for this
information collection for three (3)
years. OMB authorization for an ICR
cannot be for more than three (3) years
without renewal. The DOJ notes that
information collection requirements
submitted to the OMB for existing ICRs
receive a month-to-month extension
while they undergo review.
E:\FR\FM\02JAN1.SGM
02JAN1
]]>Agencies
[Federal Register Volume 89, Number 1 (Tuesday, January 2, 2024)]
[Notices]
[Pages 99-100]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2023-28816]
=======================================================================
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DEPARTMENT OF JUSTICE
[OMB Number 1117-0007]
Agency Information Collection Activities; Proposed eCollection
eComments Requested; Registrant Record of Controlled Substances
Destroyed
AGENCY: Drug Enforcement Administration, Department of Justice.
ACTION: 30-Day notice.
-----------------------------------------------------------------------
SUMMARY: The Drug Enforcement Administration, Department of Justice
(DOJ), will be submitting the following information collection request
to the Office of Management and Budget (OMB) for review and approval in
accordance with the Paperwork Reduction Act of 1995. This proposed
information collection was previously published in the Federal Register
on October 26, 2023, allowing for a 60-day comment period.
DATES: Comments are encouraged and will be accepted for 30 days until
February 1, 2023.
FOR FURTHER INFORMATION CONTACT: If you have comments especially on the
estimated public burden or associated response time, suggestions, or
need a copy of the proposed information collection instrument with
instructions or additional information, please contact Scott A. Brinks,
Regulatory Drafting and Policy Support Section, Drug Enforcement
Administration; Mailing Address: 8701 Morrissette Drive, Springfield,
Virginia 22152; Telephone: (571) 362-3261; email: [email protected].
SUPPLEMENTARY INFORMATION: Written comments and suggestions from the
public and affected agencies concerning the proposed collection of
information are encouraged. Your comments should address one or more of
the following four points:
--Evaluate whether the proposed collection of information is necessary
for the proper performance of the functions of the agency, including
whether the information will have practical utility;
--Evaluate the accuracy of the agency's estimate of the burden of the
proposed collection of information, including the validity of the
methodology and assumptions used;
--Enhance the quality, utility, and clarity of the information to be
collected; and/or
--Minimize the burden of the collection of information on those who are
to respond, including through the use of appropriate automated,
electronic, mechanical, or other technological collection techniques or
other forms of information technology, e.g., permitting electronic
submission of responses.
Written comments and recommendations for this information
collection should be submitted within 30 days of the publication of
this notice on the following website www.reginfo.gov/public/do/PRAMain.
Find this particular information collection by selecting ``Currently
under
[[Page 100]]
30-day Review--Open for Public Comments'' or by using the search
function and entering either the title of the information collection or
the OMB Control Number 1117-0007. This information collection request
may be viewed at www.reginfo.gov. Follow the instructions to view
Department of Justice, information collections currently under review
by OMB.
DOJ seeks PRA authorization for this information collection for
three (3) years. OMB authorization for an ICR cannot be for more than
three (3) years without renewal. The DOJ notes that information
collection requirements submitted to the OMB for existing ICRs receive
a month-to-month extension while they undergo review.
Overview of This Information Collection
1. Type of Information Collection: Extension of a currently
approved collection.
2. Title of the Form/Collection: Registrant Record of Controlled
Substances Destroyed.
3. Agency form number, if any, and the applicable component of the
Department of Justice sponsoring the collection: DEA From 41. The
applicable component within the Department of Justice is the Drug
Enforcement Administration, Diversion Control Division.
4. Affected public who will be asked or required to respond, as
well as a brief abstract:
Affected public (Primary): Private Sector--business or other for-
profit.
Affected public (Other): Not-for-profit institutions; Federal,
State, local, and tribal governments.
Abstract: In accordance with the Controlled Substance Act (CSA),
every DEA registrant must make a biennial inventory and maintain, on a
current basis, a complete and accurate record of each controlled
substance manufactured, received, sold, delivered, or otherwise
disposed of. 21 U.S.C. 827 and 958. These records must be maintained
separately from all other records of the registrant or, alternatively,
in the case of non-narcotic controlled substances, be in such form that
required information is readily retrievable from the ordinary business
records of the registrant per 21 U.S.C. 827(b)(2). The records must be
kept and be available for at least two years for inspection and copying
by officers or employees of the United States authorized by the
Attorney General. 21 U.S.C. 827(b)(3). The records must be in
accordance with and contain such relevant information as may be
required by regulations promulgated by DEA. 21 U.S.C. 827(b)(1). These
record requirements help to deter and detect diversion of controlled
substances and ensure that registrants remain accountable for all
controlled substances within their possession and/or control.
5. Obligation to Respond: Mandatory per 21 CFR 1314.
6. Total Estimated Number of Respondents: 92,832.
7. Estimated Time per Respondent: 30 minutes for DEA Form 41.
8. Frequency: DEA Form 41 is 1 per year.
9. Total Estimated Annual Time Burden: 46,416 hours.
10. Total Estimated Annual Other Costs Burden: $0.
If additional information is required, contact: Darwin Arceo,
Department Clearance Officer, Policy and Planning Staff, Justice
Management Division, United States Department of Justice, Two
Constitution Square, 145 N Street NE, 4W-218, Washington, DC 20530.
Dated: December 27, 2023.
Darwin Arceo,
Department Clearance Officer for PRA, U.S. Department of Justice.
[FR Doc. 2023-28816 Filed 12-29-23; 8:45 am]
BILLING CODE 4410-09-P
