Request for Information and Comments on Consumption of Certain Uncommon Produce Commodities in the United States; Extension of Comment Period, 71294-71295 [2020-24806]
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<![CDATA[
71294
Federal Register / Vol. 85, No. 217 / Monday, November 9, 2020 / Proposed Rules
■ 1. On page 70095, in the third
column, beginning in the 25th line,
amendatory instruction 2 is corrected to
read as follows:
§ 71.1
[Amended]
■ 2. The incorporation by reference in
14 CFR 71.1 of FAA Order 7400.11E,
Airspace Designations and Reporting
Points, dated July 21, 2020, and
effective September 15, 2020, is
amended as follows:
Paragraph 2004
Jet Routes.
*
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J–91
[Removed]
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V–119 [Amended]
From Parkersburg, WV; INT Parkersburg
067° and Indian Head, PA, 254° radials;
Indian Head; to Clarion, PA.
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V–174
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[Removed]
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[FR Doc. C1–2020–24288 Filed 11–6–20; 8:45 am]
BILLING CODE 1301–00–D
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
J–134 [Amended]
From Los Angeles, CA; Seal Beach, CA;
Thermal, CA; Parker, CA; Drake, AZ; Gallup,
NM; Cimarron, NM; Liberal, KS; Wichita, KS;
Butler, MO; St Louis, MO; to Falmouth, KY.
Food and Drug Administration
*
Request for Information and
Comments on Consumption of Certain
Uncommon Produce Commodities in
the United States; Extension of
Comment Period
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*
Paragraph 2006 United States Area
Navigation Routes.
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Q–67 SMTTH, TN to Henderson, WV
(HNN) [Amended]
SMTTH, TN WP (Lat. 35°54′41.57″ N,
long. 084°00′19.74″ W)
TONIO, KY FIX (Lat. 37°15′15.20″ N, long.
083°01′47.53″ W)
Henderson, WV (HNN) DME (Lat.
38°45′14.85″ N, long. 082°01′34.20″ W)
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Q–176 Cimarron, NM (CIM) to OTTTO, VA
[New]
Cimarron, NM (CIM) VORTAC (Lat.
36°29′29.03″ N, long. 104°52′19.20″ W)
KENTO, NM WP (Lat. 36°44′19.10″ N,
long. 103°05′57.13″ W)
Liberal, KS (LBL) VORTAC (Lat.
37°02′39.82″ N, long. 100°58′16.31″ W)
Wichita, KS (ICT) VORTAC (Lat.
37°44′42.92″ N, long. 097°35′01.79″ W)
Butler, MO (BUM) VORTAC (Lat.
38°16′19.49″ N, long. 094°29′17.74″ W)
St Louis, MO (STL) VORTAC (Lat.
38°51′38.48″ N, long. 090°28′56.52″ W)
GBEES, IN FIX (Lat. 38°41′54.72″ N, long.
085°10′13.03″ W)
BICKS, KY WP (Lat. 38°38′29.92″ N, long.
084°25′20.82″ W)
Henderson, WV (HNN) DME (Lat.
38°45′14.85″ N, long. 082°01′ 34.20″ W)
OTTTO, VA WP (Lat. 38°51′15.81″ N,
long. 078°12′20.01″ W)
*
khammond on DSKJM1Z7X2PROD with PROPOSALS
Charleston, WV. From Saginaw, MI; Alpena,
MI; to Sault Ste Marie, MI.
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Paragraph 6010(a)
Airways.
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Domestic VOR Federal
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V–45 [Amended]
From New Bern, NC; Kinston, NC; RaleighDurham, NC; INT Raleigh-Durham 275° and
Greensboro, NC, 105° radials; Greensboro;
INT Greensboro 334° and Pulaski, VA, 147°
radials; Pulaski; Bluefield, WV; to
VerDate Sep<11>2014
16:13 Nov 06, 2020
Jkt 253001
21 CFR Part 112
[Docket No. FDA–2020–N–1119]
Food and Drug Administration,
Health and Human Services (HHS).
ACTION: Notification; extension of
comment period.
AGENCY:
The Food and Drug
Administration (FDA or we) is
extending the comment period for the
notification entitled ‘‘Request for
Information and Comments on
Consumption of Certain Uncommon
Produce Commodities in the United
States’’ that appeared in the Federal
Register of August 10, 2020. We are
taking this action in response to a
request from stakeholders to extend the
comment period to allow additional
time for interested persons to develop
and submit data, information, and/or
comments for this Request for
Information.
SUMMARY:
FDA is extending the comment
period on the Request for Information
published August 10, 2020 (85 FR
48124). Submit either electronic or
written comments by January 8, 2021.
ADDRESSES: You may submit comments
as follows. Please note that late,
untimely filed comments will not be
considered. Electronic comments must
be submitted on or before January 8,
2021. The https://www.regulations.gov
electronic filing system will accept
comments until 11:59 p.m. Eastern Time
at the end of January 8, 2021. Comments
received by mail/hand delivery/courier
(for written/paper submissions) will be
considered timely if they are
postmarked or the delivery service
DATES:
PO 00000
Frm 00021
Fmt 4702
Sfmt 4702
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
confidential information that you or a
third party may not wish to be posted,
such as medical information, your or
anyone else’s Social Security number, or
confidential business information, such
as a manufacturing process. Please note
that if you include your name, contact
information, or other information that
identifies you in the body of your
comments, that information will be
posted on https://www.regulations.gov.
• If you want to submit a comment
with confidential information that you
do not wish to be made available to the
public, submit the comment as a
written/paper submission and in the
manner detailed (see ‘‘Written/Paper
Submissions’’ and ‘‘Instructions’’).
Written/Paper Submissions
Submit written/paper submissions as
follows:
• Mail/Hand Delivery/Courier (for
written/paper submissions): Dockets
Management Staff (HFA–305), Food and
Drug Administration, 5630 Fishers
Lane, Rm. 1061, Rockville, MD 20852.
• For written/paper comments
submitted to the Dockets Management
Staff, FDA will post your comment, as
well as any attachments, except for
information submitted, marked and
identified, as confidential, if submitted
as detailed in ‘‘Instructions.’’
Instructions: All submissions received
must include the Docket No. FDA–
2020–N–1119 for ‘‘Request for
Information and Comments on
Consumption of Certain Uncommon
Produce Commodities in the United
States.’’ Received comments, those filed
in a timely manner (see ADDRESSES),
will be placed in the docket and, except
for those submitted as ‘‘Confidential
Submissions,’’ publicly viewable at
https://www.regulations.gov or at the
Dockets Management Staff between 9
a.m. and 4 p.m., Monday through
Friday, 240–402–7500.
• Confidential Submissions—To
submit a comment with confidential
information that you do not wish to be
made publicly available, submit your
E:\FR\FM\09NOP1.SGM
09NOP1
Federal Register / Vol. 85, No. 217 / Monday, November 9, 2020 / Proposed Rules
comments only as a written/paper
submission. You should submit two
copies total. One copy will include the
information you claim to be confidential
with a heading or cover note that states
‘‘THIS DOCUMENT CONTAINS
CONFIDENTIAL INFORMATION.’’ The
Agency will review this copy, including
the claimed confidential information, in
its consideration of comments. The
second copy, which will have the
claimed confidential information
redacted/blacked out, will be available
for public viewing and posted on
https://www.regulations.gov. Submit
both copies to the Dockets Management
Staff. If you do not wish your name and
contact information to be made publicly
available, you can provide this
information on the cover sheet and not
in the body of your comments and you
must identify this information as
‘‘confidential.’’ Any information marked
as ‘‘confidential’’ will not be disclosed
except in accordance with 21 CFR 10.20
and other applicable disclosure law. For
more information about FDA’s posting
of comments to public dockets, see 80
FR 56469, September 18, 2015, or access
the information at: https://
www.govinfo.gov/content/pkg/FR-201509-18/pdf/2015-23389.pdf.
Docket: For access to the docket to
read background documents or the
electronic and written/paper comments
received, go to https://
www.regulations.gov and insert the
docket number, found in brackets in the
heading of this document, into the
‘‘Search’’ box and follow the prompts
and/or go to the Dockets Management
Staff, 5630 Fishers Lane, Rm. 1061,
Rockville, MD 20852, 240–402–7500.
FOR FURTHER INFORMATION CONTACT:
Samir Assar, Center for Food Safety and
Applied Nutrition (HFS–317), Food and
Drug Administration, 5001 Campus Dr.,
College Park, MD 20740, 240–402–1636.
SUPPLEMENTARY INFORMATION:
khammond on DSKJM1Z7X2PROD with PROPOSALS
I. Background
In the Federal Register of August 10,
2020 (85 FR 48124), we published a
notification entitled ‘‘Request for
Information and Comments on
Consumption of Certain Uncommon
Produce Commodities in the United
States.’’ This action opened a docket
with a 90-day comment period to
receive information and comments
related to certain produce commodities
with no or low reported consumption in
the database relied on to create the list
of rarely consumed raw commodities
that are exempt from the Standards for
the Growing, Harvesting, Packing, and
Holding of Produce for Human
VerDate Sep<11>2014
16:13 Nov 06, 2020
Jkt 253001
Consumption (21 CFR part 112)
(produce safety regulation).
FDA has received a request for a 60day extension for this comment period
in order to allow additional time for
interested persons to develop and
submit data, information, and/or
comments for this Request for
Information. We have concluded that it
is reasonable to extend for 60 days the
comment period for this Request for
Information. The Agency believes that
this extension allows adequate time for
any interested persons to submit data,
information, and/or comments for this
Request for Information.
Dated: November 3, 2020.
Lauren K. Roth,
Acting Principal Associate Commissioner for
Policy.
[FR Doc. 2020–24806 Filed 11–6–20; 8:45 am]
BILLING CODE 4164–01–P
ENVIRONMENTAL PROTECTION
AGENCY
40 CFR Part 52
[EPA–R05–OAR–2008–0784; FRL–10011–
77–Region 5]
Air Plan Approval; Wisconsin; PSD
and Nonattainment NSR Rule
Clarifications
Environmental Protection
Agency (EPA).
ACTION: Proposed rule.
AGENCY:
The Environmental Protection
Agency (EPA) is proposing to approve a
revision to the Wisconsin state
implementation plan (SIP), submitted
by the Wisconsin Department of Natural
Resources (WDNR) on September 30,
2008. The revision updates the
definition of ‘‘Replacement Unit’’ and
clarifies a component of the emission
calculation used to determine emissions
under a plantwide applicability
limitation (PAL) in the Wisconsin
Administrative Code. Approving this
revision makes Wisconsin rules
consistent with Federal rules.
DATES: Comments must be received on
or before December 9, 2020.
ADDRESSES: Submit your comments,
identified by Docket ID No. EPA–R05–
OAR–2008–0784 at https://
www.regulations.gov, or via email to
damico.genevieve@epa.gov. For
comments submitted at Regulations.gov,
follow the online instructions for
submitting comments. Once submitted,
comments cannot be edited or removed
from Regulations.gov. For either manner
of submission, EPA may publish any
comment received to its public docket.
SUMMARY:
PO 00000
Frm 00022
Fmt 4702
Sfmt 4702
71295
Do not submit electronically any
information you consider to be
Confidential Business Information (CBI)
or other information whose disclosure is
restricted by statute. Multimedia
submissions (audio, video, etc.) must be
accompanied by a written comment.
The written comment is considered the
official comment and should include
discussion of all points you wish to
make. EPA will generally not consider
comments or comment contents located
outside of the primary submission (i.e.,
on the web, cloud, or other file sharing
system). For additional submission
methods, please contact the person
identified in the FOR FURTHER
INFORMATION CONTACT section. For the
full EPA public comment policy,
information about CBI or multimedia
submissions, and general guidance on
making effective comments, please visit
https://www2.epa.gov/dockets/
commenting-epa-dockets.
FOR FURTHER INFORMATION CONTACT:
Michael Cloyd, Air Permits Section, Air
Programs Branch (AR–18J),
Environmental Protection Agency,
Region 5, 77 West Jackson Boulevard,
Chicago, Illinois 60604, (312)886–1474,
Cloyd.Michael@epa.gov. The EPA
Region 5 office is open from 8:30 a.m.
to 4:30 p.m., Monday through Friday,
excluding Federal holidays and facility
closures due to COVID 19.
SUPPLEMENTARY INFORMATION:
Throughout this document whenever
‘‘we,’’ ‘‘us,’’ or ‘‘our’’ is used, we mean
EPA.
I. Review of Wisconsin’s Submittal
This action proposes to approve the
request EPA received on September 30,
2008 from WDNR to incorporate
changes made by EPA to 40 CFR parts
51 and 52, effective on January 6, 2004
(68 FR 63021). As a result of petitions
for reconsideration, EPA added two
clarifications of underlying rules. EPA
updated the definition of ‘‘Replacement
Unit’’ to clarify that a replacement unit
is reconstructed or takes the place
completely of the unit being replaced,
the replacement unit is functionally
identical to the old unit, a replacement
unit cannot change the design
parameters of the existing process, and
the replaced unit has to be permanently
removed or rendered permanently
unusable. In addition, EPA clarified that
the PAL baseline calculation procedures
for newly constructed units do not
apply to modified units. Modified or
existing units are not considered newly
constructed units and therefore do not
need to be added to the PAL level for
the 24-month emissions period.
E:\FR\FM\09NOP1.SGM
09NOP1
]]>Agencies
[Federal Register Volume 85, Number 217 (Monday, November 9, 2020)]
[Proposed Rules]
[Pages 71294-71295]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2020-24806]
=======================================================================
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
21 CFR Part 112
[Docket No. FDA-2020-N-1119]
Request for Information and Comments on Consumption of Certain
Uncommon Produce Commodities in the United States; Extension of Comment
Period
AGENCY: Food and Drug Administration, Health and Human Services (HHS).
ACTION: Notification; extension of comment period.
-----------------------------------------------------------------------
SUMMARY: The Food and Drug Administration (FDA or we) is extending the
comment period for the notification entitled ``Request for Information
and Comments on Consumption of Certain Uncommon Produce Commodities in
the United States'' that appeared in the Federal Register of August 10,
2020. We are taking this action in response to a request from
stakeholders to extend the comment period to allow additional time for
interested persons to develop and submit data, information, and/or
comments for this Request for Information.
DATES: FDA is extending the comment period on the Request for
Information published August 10, 2020 (85 FR 48124). Submit either
electronic or written comments by January 8, 2021.
ADDRESSES: You may submit comments as follows. Please note that late,
untimely filed comments will not be considered. Electronic comments
must be submitted on or before January 8, 2021. The https://www.regulations.gov electronic filing system will accept comments until
11:59 p.m. Eastern Time at the end of January 8, 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 confidential information that you or a third party
may not wish to be posted, such as medical information, your or anyone
else's Social Security number, or confidential business information,
such as a manufacturing process. Please note that if you include your
name, contact information, or other information that identifies you in
the body of your comments, that information will be posted on https://www.regulations.gov.
If you want to submit a comment with confidential
information that you do not wish to be made available to the public,
submit the comment as a written/paper submission and in the manner
detailed (see ``Written/Paper Submissions'' and ``Instructions'').
Written/Paper Submissions
Submit written/paper submissions as follows:
Mail/Hand Delivery/Courier (for written/paper
submissions): Dockets Management Staff (HFA-305), Food and Drug
Administration, 5630 Fishers Lane, Rm. 1061, Rockville, MD 20852.
For written/paper comments submitted to the Dockets
Management Staff, FDA will post your comment, as well as any
attachments, except for information submitted, marked and identified,
as confidential, if submitted as detailed in ``Instructions.''
Instructions: All submissions received must include the Docket No.
FDA-2020-N-1119 for ``Request for Information and Comments on
Consumption of Certain Uncommon Produce Commodities in the United
States.'' Received comments, those filed in a timely manner (see
ADDRESSES), will be placed in the docket and, except for those
submitted as ``Confidential Submissions,'' publicly viewable at https://www.regulations.gov or at the Dockets Management Staff between 9 a.m.
and 4 p.m., Monday through Friday, 240-402-7500.
Confidential Submissions--To submit a comment with
confidential information that you do not wish to be made publicly
available, submit your
[[Page 71295]]
comments only as a written/paper submission. You should submit two
copies total. One copy will include the information you claim to be
confidential with a heading or cover note that states ``THIS DOCUMENT
CONTAINS CONFIDENTIAL INFORMATION.'' The Agency will review this copy,
including the claimed confidential information, in its consideration of
comments. The second copy, which will have the claimed confidential
information redacted/blacked out, will be available for public viewing
and posted on https://www.regulations.gov. Submit both copies to the
Dockets Management Staff. If you do not wish your name and contact
information to be made publicly available, you can provide this
information on the cover sheet and not in the body of your comments and
you must identify this information as ``confidential.'' Any information
marked as ``confidential'' will not be disclosed except in accordance
with 21 CFR 10.20 and other applicable disclosure law. For more
information about FDA's posting of comments to public dockets, see 80
FR 56469, September 18, 2015, or access the information at: https://www.govinfo.gov/content/pkg/FR-2015-09-18/pdf/2015-23389.pdf.
Docket: For access to the docket to read background documents or
the electronic and written/paper comments received, go to https://www.regulations.gov and insert the docket number, found in brackets in
the heading of this document, into the ``Search'' box and follow the
prompts and/or go to the Dockets Management Staff, 5630 Fishers Lane,
Rm. 1061, Rockville, MD 20852, 240-402-7500.
FOR FURTHER INFORMATION CONTACT: Samir Assar, Center for Food Safety
and Applied Nutrition (HFS-317), Food and Drug Administration, 5001
Campus Dr., College Park, MD 20740, 240-402-1636.
SUPPLEMENTARY INFORMATION:
I. Background
In the Federal Register of August 10, 2020 (85 FR 48124), we
published a notification entitled ``Request for Information and
Comments on Consumption of Certain Uncommon Produce Commodities in the
United States.'' This action opened a docket with a 90-day comment
period to receive information and comments related to certain produce
commodities with no or low reported consumption in the database relied
on to create the list of rarely consumed raw commodities that are
exempt from the Standards for the Growing, Harvesting, Packing, and
Holding of Produce for Human Consumption (21 CFR part 112) (produce
safety regulation).
FDA has received a request for a 60-day extension for this comment
period in order to allow additional time for interested persons to
develop and submit data, information, and/or comments for this Request
for Information. We have concluded that it is reasonable to extend for
60 days the comment period for this Request for Information. The Agency
believes that this extension allows adequate time for any interested
persons to submit data, information, and/or comments for this Request
for Information.
Dated: November 3, 2020.
Lauren K. Roth,
Acting Principal Associate Commissioner for Policy.
[FR Doc. 2020-24806 Filed 11-6-20; 8:45 am]
BILLING CODE 4164-01-P
