Agency Information Collection Activities; Proposed eCollection eComments Requested; Extension of a Previously Approved Collection; Drug Use Statement, 22742-22743 [2024-06955]

Download as PDF khammond on DSKJM1Z7X2PROD with NOTICES 22742 Federal Register / Vol. 89, No. 64 / Tuesday, April 2, 2024 / Notices to cease and desist orders. (19 U.S.C. 1337(f)(1)). The Commission is soliciting submissions on public interest issues raised by the recommended relief should the Commission find a violation, specifically: a general exclusion order directed to certain blood flow restriction devices with rotatable windlasses and components thereof that infringe claims 1, 4, 15, and 16 of U.S. Patent No. 7,842,067 (‘‘the ’067 patent’’) that are imported, sold for importation, and/or sold after importation; a limited exclusion order directed to certain blood flow restriction devices with rotatable windlasses and components thereof that infringe claims 1, 4, 15, and 16 of the ’067 patent, infringe U.S. Trademark Registration Nos. 3,863,064 and 5,046,378, and/or infringe the asserted Trade Dress and that are imported, sold for importation, and/or sold after importation by Respondents Anping Longji Medical Equipment Factory; Dongguanwin Si Hai Precision Mold Co., Ltd.; Eiffel Medical Supplies Co., Ltd.; Empire State Distributors Inc.; EMRN Medical Equipment; GD Tianwu New Material Tech Co., Ltd.; Hengshui Runde Medical Instruments Co., Ltd.; Putian Dima Trading Co., Ltd.; Rhino Inc.; Shanghai Sixu International Freight Agent Co., Ltd.; Shenzhen Anben E-Commerce Co., Ltd.; Shenzhen TMI Medical Supplies Co., Ltd.; Shenzhen Yujie Commercial and Trading Co., Ltd.; Wuxi Emsrun Technology Co., Ltd.; Wuxi Golden Hour Medical Technology Co., Ltd.; and Wuxi Puneda Technology Co., Ltd. (collectively, ‘‘Defaulting Respondents’’); and cease and desist orders directed to each Defaulting Respondent. Parties are to file public interest submissions pursuant to 19 CFR 210.50(a)(4). The Commission is interested in further development of the record on the public interest in this investigation. Accordingly, members of the public and interested government agencies are invited to file submissions of no more than five (5) pages, inclusive of attachments, concerning the public interest in light of the ALJ’s Recommended Determination on Remedy and Bond issued in this investigation on March 19, 2024. Comments should address whether issuance of the recommended remedial orders in this investigation would affect the public health and welfare in the United States, competitive conditions in the United States economy, the production of like or directly competitive articles in the United States, or United States consumers. VerDate Sep<11>2014 17:06 Apr 01, 2024 Jkt 262001 In particular, the Commission is interested in comments that: (i) explain how the articles potentially subject to the recommended remedial orders are used in the United States; (ii) identify any public health, safety, or welfare concerns in the United States relating to the recommended orders; (iii) identify like or directly competitive articles that complainant, its licensees, or third parties make in the United States which could replace the subject articles if they were to be excluded; (iv) indicate whether complainant, complainant’s licensees, and/or thirdparty suppliers have the capacity to replace the volume of articles potentially subject to the recommended orders within a commercially reasonable time; and (v) explain how the recommended orders would impact consumers in the United States. Written submissions must be filed no later than by close of business on April 26, 2024. Persons filing written submissions must file the original document electronically on or before the deadlines stated above. The Commission’s paper filing requirements in 19 CFR 210.4(f) are currently waived. 85 FR 15798 (Mar. 19, 2020). Submissions should refer to the investigation number (‘‘Inv. No. 337–TA–1364’’) in a prominent place on the cover page and/or the first page. (See Handbook for Electronic Filing Procedures, https://www.usitc.gov/ secretary/fed_reg_notices/rules/ handbook_on_electronic_filing.pdf). Persons with questions regarding filing should contact the Secretary (202–205– 2000). Any person desiring to submit a document to the Commission in confidence must request confidential treatment by marking each document with a header indicating that the document contains confidential information. This marking will be deemed to satisfy the request procedure set forth in Rules 201.6(b) and 210.5(e)(2) (19 CFR 201.6(b) & 210.5(e)(2)). Documents for which confidential treatment by the Commission is properly sought will be treated accordingly. Any non-party wishing to submit comments containing confidential information must serve those comments on the parties to the investigation pursuant to the applicable Administrative Protective Order. A redacted non-confidential version of the document must also be filed simultaneously with any confidential filing and must be served in accordance with Commission Rule 210.4(f)(7)(ii)(A) (19 CFR 210.4(f)(7)(ii)(A)). All PO 00000 Frm 00080 Fmt 4703 Sfmt 4703 information, including confidential business information and documents for which confidential treatment is properly sought, submitted to the Commission for purposes of this investigation may be disclosed to and used: (i) by the Commission, its employees and Offices, and contract personnel (a) for developing or maintaining the records of this or a related proceeding, or (b) in internal investigations, audits, reviews, and evaluations relating to the programs, personnel, and operations of the Commission including under 5 U.S.C. Appendix 3; or (ii) by U.S. government employees and contract personnel, solely for cybersecurity purposes. All contract personnel will sign appropriate nondisclosure agreements. All nonconfidential written submissions will be available for public inspection on EDIS. This action is taken under the authority of section 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: March 25, 2024. Katherine Hiner, Supervisory Attorney. [FR Doc. 2024–06897 Filed 4–1–24; 8:45 am] BILLING CODE 7020–02–P DEPARTMENT OF JUSTICE [OMB Number 1117–0043] Agency Information Collection Activities; Proposed eCollection eComments Requested; Extension of a Previously Approved Collection; Drug Use Statement Drug Enforcement Administration, Department of Justice. ACTION: 30-Day notice. AGENCY: 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. The proposed information collection was previously published in the Federal Register on December 24, 2024 allowing a 60-day comment period. DATES: Comments are encouraged and will be accepted for 30 days until June 3, 2024. FOR FURTHER INFORMATION CONTACT: If you have additional comments especially on the estimated public SUMMARY: E:\FR\FM\02APN1.SGM 02APN1 Federal Register / Vol. 89, No. 64 / Tuesday, April 2, 2024 / Notices burden or associated response time, suggestions, or need a copy of the proposed information collection instrument with instructions or additional information, please contact Kannessia Jordan, Section Chief, Office of Compliance, Policy Administration Section, 700 Army Navy Drive, Arlington, VA 22202, telephone: 571– 776–2262, email: Kannessia.S.Jordan@ DEA.gov. 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 Bureau of Justice Statistics, 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; —Evaluate whether and if so how the quality, utility, and clarity of the information to be collected can be enhanced; and —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. khammond on DSKJM1Z7X2PROD with NOTICES SUPPLEMENTARY INFORMATION: 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 1117–0043. 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 VerDate Sep<11>2014 17:06 Apr 01, 2024 Jkt 262001 receive a month-to-month extension while they undergo review. NATIONAL AERONAUTICS AND SPACE ADMINISTRATION Overview of This Information Collection [Notice: 024–025] 1. Type of Information Collection: Extension of a previously approved collection. 2. The Title of the Form/Collection: Drug Questionnaire. 3. The agency form number, if any, and the applicable component of the Department sponsoring the collection: Form number: DEA–341 (Common Form). The sponsoring component is the Drug Enforcement Administration. 4. Affected public who will be asked or required to respond, as well as the obligation to respond: Affected Public: Individuals or households. Abstract: This collection requires the drug history of any individual seeking employment with DEA. DEA policy states that a past history of illegal drug use may result in ineligibility for employment. The form asks job applicants specific questions about their personal history, if any, of illegal drug use. 5. The obligation to respond is voluntary but applications will not be reviewed without the completion of the form. 6. An estimate of the total number of respondents: The total or estimated number of respondents for the Drug Questionnaire is 4,727. 7. The amount of time estimated for an average respondent to respond: The time per response is seven minutes. 8. Frequency: 1 per application or selection. 9. An estimate of the total annual burden (in hours) associated with the collection: The total annual burden hours for this collection is 551 hours. 10. An estimate of the total annual cost burden associated with the collection, if applicable: $0. If additional information is required contact: Darwin Arceo, Department Clearance Officer, United States Department of Justice, Justice Management Division, Policy and Planning Staff, Two Constitution Square, 145 N Street NE, 4W–218, Washington, DC. Dated: March 25, 2024. Darwin Arceo, Department Clearance Officer for PRA, U.S. Department of Justice. [FR Doc. 2024–06955 Filed 4–1–24; 8:45 am] BILLING CODE 4410–09–P PO 00000 Frm 00081 Fmt 4703 Sfmt 4703 22743 Aerospace Safety Advisory Panel; Meeting. National Aeronautics and Space Administration (NASA). ACTION: Notice of meeting. AGENCY: In accordance with the Federal Advisory Committee Act, as amended, the National Aeronautics and Space Administration announces a forthcoming meeting of the Aerospace Safety Advisory Panel (ASAP). The ASAP will hold its Second Quarterly Meeting for 2024. This discussion is pursuant to carrying out its statutory duties for which the Panel reviews, identifies, evaluates, and advises on those program activities, systems, procedures, and management activities that can contribute to program risk. Priority is given to those programs that involve the safety of human flight. DATES: Wednesday, April 17, 2024, 3 p.m. to 4:30 p.m., central time. ADDRESSES: Public attendance will be virtual only. See dial-in information below under SUPPLEMENTARY INFORMATION. SUMMARY: Ms. Lisa M. Hackley, ASAP Administrative Officer, NASA Headquarters, Washington, DC 20546, (202) 358–1947 or lisa.m.hackley@nasa.gov. SUPPLEMENTARY INFORMATION: As noted above, this meeting is only available telephonically. Any interested person must use a touch-tone phone to participate in this meeting. Any interested person may call the USA toll free conference call number 888–566– 6133; passcode 8343253 and then the # sign. At the beginning of the meeting, members of the public may make a verbal presentation to the Panel limited to the subject of safety in NASA, not to exceed 5 minutes in length. To do so, members of the public must contact Ms. Lisa M. Hackley at lisa.m.hackley@ nasa.gov or at (202) 358–1947 at least 48 hours in advance. Any member of the public is permitted to file a written statement with the Panel via electronic submission to Ms. Hackley at the email address previously noted. Written statements should be limited to the subject of safety in NASA. The agenda for the meeting includes the following topics: —Updates on the International Space Station Program —Updates on the Commercial Crew Program FOR FURTHER INFORMATION CONTACT: E:\FR\FM\02APN1.SGM 02APN1

Agencies

Department of Justice

[Federal Register Volume 89, Number 64 (Tuesday, April 2, 2024)]
[Notices]
[Pages 22742-22743]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2024-06955]


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DEPARTMENT OF JUSTICE

[OMB Number 1117-0043]


Agency Information Collection Activities; Proposed eCollection 
eComments Requested; Extension of a Previously Approved Collection; 
Drug Use Statement

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. The proposed 
information collection was previously published in the Federal Register 
on December 24, 2024 allowing a 60-day comment period.

DATES: Comments are encouraged and will be accepted for 30 days until 
June 3, 2024.

FOR FURTHER INFORMATION CONTACT: If you have additional comments 
especially on the estimated public

[[Page 22743]]

burden or associated response time, suggestions, or need a copy of the 
proposed information collection instrument with instructions or 
additional information, please contact Kannessia Jordan, Section Chief, 
Office of Compliance, Policy Administration Section, 700 Army Navy 
Drive, Arlington, VA 22202, telephone: 571-776-2262, 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 Bureau of Justice 
Statistics, 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;
--Evaluate whether and if so how the quality, utility, and clarity of 
the information to be collected can be enhanced; and
--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 1117-0043. 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 previously 
approved collection.
    2. The Title of the Form/Collection: Drug Questionnaire.
    3. The agency form number, if any, and the applicable component of 
the Department sponsoring the collection: Form number: DEA-341 (Common 
Form). The sponsoring component is the Drug Enforcement Administration.
    4. Affected public who will be asked or required to respond, as 
well as the obligation to respond: Affected Public: Individuals or 
households. Abstract: This collection requires the drug history of any 
individual seeking employment with DEA. DEA policy states that a past 
history of illegal drug use may result in ineligibility for employment. 
The form asks job applicants specific questions about their personal 
history, if any, of illegal drug use.
    5. The obligation to respond is voluntary but applications will not 
be reviewed without the completion of the form.
    6. An estimate of the total number of respondents: The total or 
estimated number of respondents for the Drug Questionnaire is 4,727.
    7. The amount of time estimated for an average respondent to 
respond: The time per response is seven minutes.
    8. Frequency: 1 per application or selection.
    9. An estimate of the total annual burden (in hours) associated 
with the collection: The total annual burden hours for this collection 
is 551 hours.
    10. An estimate of the total annual cost burden associated with the 
collection, if applicable: $0.
    If additional information is required contact: Darwin Arceo, 
Department Clearance Officer, United States Department of Justice, 
Justice Management Division, Policy and Planning Staff, Two 
Constitution Square, 145 N Street NE, 4W-218, Washington, DC.

    Dated: March 25, 2024.
Darwin Arceo,
Department Clearance Officer for PRA, U.S. Department of Justice.
[FR Doc. 2024-06955 Filed 4-1-24; 8:45 am]
BILLING CODE 4410-09-P

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