Agency Information Collection Activities; Announcement of Office of Management and Budget Approvals, 77469 [2020-26571]
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77469
Federal Register / Vol. 85, No. 232 / Wednesday, December 2, 2020 / Notices
final rule for any proposal to amend the
standard of identity for canned Pacific
salmon that may result from the
National Food Processors Association’s
petition, submitted on behalf of Bumble
Bee Seafoods, Inc., and other salmon
packers holding temporary permits, or
30 days after termination of such
proposal.
In the Federal Register of April 24,
2020 (85 FR 23047), we issued a notice
announcing that we amended the
temporary permit to allow for the
canned skinless and boneless chunk
salmon packed in water with or without
sodium tripolyphosphate and to allow
the test product to be manufactured
only at one plant, Pataya Food
Industries Ltd., located at 90/6 Moo 7,
Settakit Road, Tambol Tarsai, Amphur
Maung, Samutsakorn 74000, Thailand.
Under our regulations at 21 CFR
130.17(f), we are amending the
temporary permit issued to Bumble Bee
Seafoods, Inc., to allow the test product
to be manufactured at an additional
plant, RS Cannery Company Limited,
located at 255/1 Industrial Soi 3,
Bangpoo Industrial Estate,
Samutprakarn 10280, Thailand. All
other conditions and terms of this
permit remain the same.
Dated: November 23, 2020.
Lauren K. Roth,
Acting Principal Associate Commissioner for
Policy.
[FR Doc. 2020–26533 Filed 12–1–20; 8:45 am]
BILLING CODE 4164–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket Nos. FDA–2013–N–1119; FDA–
2010–N–0622; FDA–2011–N–0016; FDA–
2009–N–0501; and FDA–2019–N–6098]
Agency Information Collection
Activities; Announcement of Office of
Management and Budget Approvals
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Notice.
The Food and Drug
Administration (FDA) is publishing a
SUMMARY:
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, Office of Operations, Food
and Drug Administration, Three White
Flint North, 10A–12M, 11601
Landsdown St., North Bethesda, MD
20852, 301–796–7726, PRAStaff@
fda.hhs.gov.
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 https://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.
SUPPLEMENTARY INFORMATION:
TABLE 1—LIST OF INFORMATION COLLECTIONS APPROVED BY OMB
OMB
control No.
Title of collection
Food Canning Establishment Registration, Process Filing and Recordkeeping for Acidified and Thermally Processed Low-Acid Foods .........................................................................................................................................
Color Additive Certification Requests and Recordkeeping .....................................................................................
Recordkeeping and Records Access Requirements for Food Facilities .................................................................
Reporting and Recordkeeping Requirements for Reportable Food ........................................................................
Focus Groups as Used by the Food and Drug Administration ...............................................................................
Dated: November 25, 2020.
Lauren K. Roth,
Acting Principal Associate Commissioner for
Policy.
[FR Doc. 2020–26571 Filed 12–1–20; 8:45 am]
BILLING CODE 4164–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2010–N–0190]
Agency Information Collection
Activities; Proposed Collection;
Comment Request; Infant Formula
Requirements
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Notice.
The Food and Drug
Administration (FDA or Agency) is
announcing an opportunity for public
comment on the proposed collection of
SUMMARY:
VerDate Sep<11>2014
17:39 Dec 01, 2020
Jkt 253001
certain information by the Agency.
Under the Paperwork Reduction Act of
1995 (PRA), Federal Agencies are
required to publish notice in the
Federal Register concerning each
proposed collection of information,
including each proposed extension of an
existing collection of information, and
to allow 60 days for public comment in
response to the notice. This notice
solicits comments on the information
collection provisions of our infant
formula regulations, including infant
formula labeling, quality control
procedures, notification requirements,
and recordkeeping. The notice also
invites comment on electronic Form
FDA 3978 that allows manufacturers of
infant formula to submit reports and
notifications in a standardized format.
DATES: Submit either electronic or
written comments on the collection of
information by February 1, 2021.
ADDRESSES: You may submit comments
as follows. Please note that late,
untimely filed comments will not be
PO 00000
Frm 00045
Fmt 4703
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0910–0037
0910–0216
0910–0560
0910–0643
0910–0497
Date approval
expires
10/31/2023
10/31/2023
10/31/2023
10/31/2023
11/30/2023
considered. Electronic comments must
be submitted on or before February 1,
2021. The https://www.regulations.gov
electronic filing system will accept
comments until 11:59 p.m. Eastern Time
at the end of February 1, 2021.
Comments received by mail/hand
delivery/courier (for written/paper
submissions) will be considered timely
if they are postmarked or the delivery
service acceptance receipt is on or
before that date.
Electronic Submissions
Submit electronic comments in the
following way:
• Federal eRulemaking Portal:
https://www.regulations.gov. Follow the
instructions for submitting comments.
Comments submitted electronically,
including attachments, to https://
www.regulations.gov will be posted to
the docket unchanged. Because your
comment will be made public, you are
solely responsible for ensuring that your
comment does not include any
E:\FR\FM\02DEN1.SGM
02DEN1
]]>Agencies
[Federal Register Volume 85, Number 232 (Wednesday, December 2, 2020)]
[Notices]
[Page 77469]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2020-26571]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
[Docket Nos. FDA-2013-N-1119; FDA-2010-N-0622; FDA-2011-N-0016; FDA-
2009-N-0501; and FDA-2019-N-6098]
Agency Information Collection Activities; Announcement of Office
of Management and Budget Approvals
AGENCY: Food and Drug Administration, HHS.
ACTION: Notice.
-----------------------------------------------------------------------
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, Office of Operations,
Food and Drug Administration, Three White Flint North, 10A-12M, 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
https://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
------------------------------------------------------------------------
OMB control Date approval
Title of collection No. expires
------------------------------------------------------------------------
Food Canning Establishment Registration, 0910-0037 10/31/2023
Process Filing and Recordkeeping for
Acidified and Thermally Processed Low-
Acid Foods.............................
Color Additive Certification Requests 0910-0216 10/31/2023
and Recordkeeping......................
Recordkeeping and Records Access 0910-0560 10/31/2023
Requirements for Food Facilities.......
Reporting and Recordkeeping Requirements 0910-0643 10/31/2023
for Reportable Food....................
Focus Groups as Used by the Food and 0910-0497 11/30/2023
Drug Administration....................
------------------------------------------------------------------------
Dated: November 25, 2020.
Lauren K. Roth,
Acting Principal Associate Commissioner for Policy.
[FR Doc. 2020-26571 Filed 12-1-20; 8:45 am]
BILLING CODE 4164-01-P
