[Federal Register Volume 82, Number 100 (Thursday, May 25, 2017)]
[Notices]
[Page 24136]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2017-10711]


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DEPARTMENT OF HEALTH AND HUMAN SERVICES

Food and Drug Administration

[Docket Nos. FDA-2013-N-1423; FDA-2013-N-0730; FDA-2012-N-0977; FDA-
2013-N-0557; FDA-2009-N-0380; FDA-2013-N-0514; FDA-2013-N-0190; FDA-
2010-D-0350; FDA-2016-N-0538; FDA-2013-N-1428]


Agency Information Collection Activities; Announcement of Office 
of Management and Budget Approvals

AGENCY: Food and Drug Administration, HHS.

ACTION: Notice.

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SUMMARY: The Food and Drug Administration (FDA) is publishing a list of 
information collections that have been approved by the Office of 
Management and Budget (OMB) under the Paperwork Reduction Act of 1995.

FOR FURTHER INFORMATION CONTACT: Ila S. Mizrachi, FDA PRA Staff, Office 
of Operations, Food and Drug Administration, Three White Flint North, 
11601 Landsdown St., North Bethesda, MD 20852, 301-796-7726, 
[email protected].

SUPPLEMENTARY INFORMATION: The following is a list of FDA information 
collections recently approved by OMB under section 3507 of the 
Paperwork Reduction Act of 1995 (44 U.S.C. 3507). The OMB control 
number and expiration date of OMB approval for each information 
collection are shown in table 1. Copies of the supporting statements 
for the information collections are available on the Internet at http://www.reginfo.gov/public/do/PRAMain. An Agency may not conduct or 
sponsor, and a person is not required to respond to, a collection of 
information unless it displays a currently valid OMB control number.

        Table 1--List of Information Collections Approved by OMB
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                                            OMB control    Date approval
           Title of collection                  No.           expires
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Importer's Entry Notice.................       0910-0046      12/31/2019
Threshold of Regulation for Substances         0910-0298      12/31/2019
 Used in Food-Contact Articles..........
Regulations Restricting the Sale and           0910-0312      12/31/2019
 Distribution of Cigarettes and
 Smokeless Tobacco to Protect Children
 and Adolescents........................
Postmarket Surveillance of Medical             0910-0449      12/31/2019
 Devices................................
Product Jurisdiction: Assignment of            0910-0523      12/31/2019
 Agency Component for Review of
 Premarket Applications.................
Administrative Procedures for Clinical         0910-0607      12/31/2019
 laboratory Improvement Amendments of
 1988 Categorization (42 CFR 493.17)....
Requirements under the Comprehensive           0910-0671      12/31/2019
 Smokeless Tobacco Health Education Act
 of 1986; as amended by the Family
 Smoking Prevention and Tobacco Control
 Act....................................
Guidance for Industry on Tobacco               0910-0745      12/31/2019
 Retailer Training Programs.............
Animation in Direct-to-Consumer                0910-0826      12/31/2019
 Advertising............................
Guidance for Industry: Electronic Drug         0910-0827      12/31/2019
 Product Reporting for Human Drug
 Compounding Outsourcing Facilities
 Under Section 503B of the Federal Food,
 Drug, and Cosmetic Act.................
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    Dated: May 18, 2017.
Anna K. Abram,
Deputy Commissioner for Policy, Planning, Legislation, and Analysis.
[FR Doc. 2017-10711 Filed 5-24-17; 8:45 am]
BILLING CODE 4164-01-P