30 Day FRN

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Federal Register / Vol. 88, No. 220 / Thursday, November 16, 2023 / Notices
respect to the asserted ’026 mark. No
party petitioned for review of the ID.
On September 19, 2022, the
Commission determined not to review
the RID. 87 FR 58130–1 (Sept. 23, 2022).
On November 15, 2022, the Commission
issued a final determination finding a
violation, issuing a GEO prohibiting the
unlicensed importation of chocolate
milk powder and packaging thereof that
infringe the ’026 mark, and terminating
the investigation. 87 FR 70864–65. On
the same day, the Commission issued an
opinion explaining the basis for its final
determination.
On October 9, 2023, Meenaxi filed a
complaint requesting that the
Commission institute an enforcement
proceeding under Commission Rule
210.75 to investigate alleged violations
of the General Exclusion Order by four
proposed enforcement respondents: (1)
Organic Ingredients; (2) New India; (3)
Bharat Bazar; and (4) Coconut Hill Inc.
of Sunnyvale, California. Meenaxi
asserts that the four proposed
enforcement respondents continue to
import, sell for importation, advertise,
market, distribute, offer to sell
‘‘Bournvita’’ products that infringe the
‘026 mark. Meenaxi also alleges that the
four proposed enforcement respondents
are in continuing violation of the GEO
and as a result, it is sustaining
‘‘immediate and irreparable harm.’’
None of the respondents answered
Meenaxi’s enforcement complaint.
Having examined the enforcement
complaint and the supporting
documents, the Commission has
determined to institute a formal
enforcement proceeding, pursuant to
Commission Rule 210.75(a) (19 CFR
210.75(a)), to determine whether
violations of the GEO, issued on
November 15, 2022 in the abovereferenced investigation, have occurred
and to determine what, if any,
enforcement measures are appropriate.
The named respondents are: (1) Organic
Ingredients Inc. d/b/a Namaste Plaza
Indian Super Market; (2) New India
Bazar Inc.; (3) Bharat Bazar Inc.; and (4)
Coconut Hill Inc. d/b/a Coconut Hill.
OUII is also named as a party.
In the Order issued concurrently
herewith, the Commission has delegated
this enforcement proceeding to the CALJ
for designation of a presiding
Administrative Law Judge to conduct
any necessary proceedings, issue an
Enforcement Initial Determination, and
make a recommendation on appropriate
enforcement measures, if any.
The Commission’s vote on this
determination took place on November
9, 2023.
The authority for the Commission’s
determination is contained in section

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337 of the Tariff Act of 1930, as
amended (19 U.S.C. 1337), and in part
210 of the Commission’s Rules of
Practice and Procedure (19 CFR part
210).
By order of the Commission.
Issued: November 9, 2023.
Lisa Barton,
Secretary to the Commission.
[FR Doc. 2023–25279 Filed 11–15–23; 8:45 am]
BILLING CODE 7020–02–P

INTERNATIONAL TRADE
COMMISSION
[Investigation Nos. 701–TA–683 and 731–
TA–1594–1596 (Final)]

Paper File Folders From China, India,
and Vietnam
Determinations
On the basis of the record 1 developed
in the subject investigations, the United
States International Trade Commission
(‘‘Commission’’) determines, pursuant
to the Tariff Act of 1930 (‘‘the Act’’),
that an industry in the United States is
materially injured by reason of imports
of paper file folders from China, India,
and Vietnam, provided for in
subheading 4820.30.00 of the
Harmonized Tariff Schedule of the
United States, that have been found by
the U.S. Department of Commerce
(‘‘Commerce’’) to be sold in the United
States at less than fair value (‘‘LTFV’’),
and to be subsidized by the government
of India.2
Background
The Commission instituted these
investigations, effective October 12,
2022, following receipt of petitions filed
with the Commission and Commerce by
the Coalition of Domestic Folder
Manufacturers, Hastings, Minnesota and
Naperville, Illinois. The final phase of
the investigations was scheduled by the
Commission following notification of
preliminary determinations by
Commerce that imports of paper file
folders from India were subsidized
within the meaning of section 703(b) of
the Act (19 U.S.C. 1671b(b)) and imports
of paper file folders from China, India,
and Vietnam were sold at LTFV within
the meaning of 733(b) of the Act (19
U.S.C. 1673b(b)). Notice of the
scheduling of the final phase of the
Commission’s investigations and of a
public hearing to be held in connection
therewith was given by posting copies
1 The record is defined in § 207.2(f) of the
Commission’s Rules of Practice and Procedure (19
CFR 207.2(f)).
2 88 FR 69130, 88 FR 69134, 88 FR 69138, and
88 FR 69141, October 5, 2023.

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of the notice in the Office of the
Secretary, U.S. International Trade
Commission, Washington, DC, and by
publishing the notice in the Federal
Register on June 8, 2023 (88 FR 37579).
The public hearing in connection with
the investigations, originally scheduled
for October 3, 2023, was cancelled.3
The Commission made these
determinations pursuant to §§ 705(b)
and 735(b) of the Act (19 U.S.C.
1671d(b) and 19 U.S.C. 1673d(b)). It
completed and filed its determinations
in these investigations on November 13,
2023. The views of the Commission are
contained in USITC Publication 5472
(November 2023), entitled Paper File
Folders from China, India, and Vietnam:
Investigation Nos. 701–TA–683 and
731–TA–1594–1596 (Final).
By order of the Commission.
Issued: November 13, 2023.
Lisa Barton,
Secretary to the Commission.
[FR Doc. 2023–25331 Filed 11–15–23; 8:45 am]
BILLING CODE 7020–02–P

DEPARTMENT OF JUSTICE
[OMB Number 1117–0023]

Agency Information Collection
Activities; Proposed eCollection
eComments Requested; Import/Export
Declaration for List I and List II
Chemical
Drug Enforcement
Administration, Department of Justice.
ACTION: 30-Day notice.
AGENCY:

SUMMARY: 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
September 11, 2023, allowing for a 60day comment period.
DATES: Comments are encouraged and
will be accepted for 30 days until
December 18, 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,
3 88

FR 68670, October 4, 2023.

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lotter on DSK11XQN23PROD with NOTICES1

78788

Federal Register / Vol. 88, No. 220 / Thursday, November 16, 2023 / Notices

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
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 1117–0023. 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.

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2. Title of the Form/Collection:
Import/Export Declaration for List I and
List II Chemicals.
3. Agency form number, if any, and
the applicable component of the
Department of Justice sponsoring the
collection: DEA Forms: 486, 486A. 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):
Business or other for-profit. Affected
public (Other): Not-for-profit
institutions; Federal, State, local, and
tribal governments.
Abstract: Section 1018 of the
Controlled Substances Import and
Export Act (CSIEA) (21 U.S.C. 971) and
Title 21 Code of Federal Regulations (21
CFR) Part 1313 require any persons who
import, export, or conduct international
transactions involving list I and list II
chemicals are required to establish a
system of recordkeeping and report
certain information regarding those
transactions to DEA. The chemicals
subject to control are used in the
clandestine manufacture of controlled
substances. The reports of domestic,
import, and export regulated
transactions in listed chemicals are
submitted electronically through the
Diversion Control Division secure
network application. Any person who
desires to import non-narcotic
substances in schedules III, IV, and V
must electronically file their return
information. Any person who desires to
export non-narcotic substances in
schedules III and IV and any other
substance in schedule V is also required
to electronically file a controlled
substances import declaration/
controlled substance export invoice.
5. Obligation to Respond: Mandatory
per 21 CFR 1313.
6. Total Estimated Number of
Respondents: 631.
7. Estimated Time per Respondent: 11
minutes for DEA–486 Import, DEA–486
International, and DEA–486A Import,
and 12 minutes for DEA–486 Export.
8. Frequency: 1 for DEA–486 Import
and DEA–486A Import, 4 for DEA–486
International, and 77 for DEA–486
Export.
9. Total Estimated Annual Time
Burden: Ex: 4,134 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,

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Two Constitution Square, 145 N Street
NE, 4W–218 Washington, DC 20530.
Dated: November 7, 2023.
Darwin Arceo,
Department Clearance Officer for PRA, U.S.
Department of Justice.
[FR Doc. 2023–25326 Filed 11–15–23; 8:45 am]
BILLING CODE 4410–09–P

DEPARTMENT OF JUSTICE
[OMB Number 1117–0013]

Agency Information Collection
Activities; Proposed eCollection
eComments Requested; Application
for Permit To Import Controlled
Substances for Domestic and/or
Scientific Purposes
Drug Enforcement
Administration, Department of Justice.
ACTION: 30-Day notice.
AGENCY:

SUMMARY: 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
September 11, 2023, allowing for a 60day comment period.
DATES: Comments are encouraged and
will be accepted for 30 days until
December 18, 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

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