Standards for the Growing, Harvesting, Packing, and Holding of Produce for Human Consumption: What You Need To Know About the Food and Drug Administration Regulation; Small Entity Compliance Guide; Availability, 42031-42032 [2017-18811]
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Federal Register / Vol. 82, No. 171 / Wednesday, September 6, 2017 / Rules and Regulations
Standards Branch, FAA, has the authority to
approve AMOCs for this AD, if requested
using the procedures found in 14 CFR 39.19.
Send information to ATTN: Mike Kiesov,
Aerospace Engineer, Small Airplane
Standards Branch, FAA 901 Locust, Room
301, Kansas City, Missouri 64106; telephone:
(816) 329–4144; fax: (816) 329–4090; email:
mike.kiesov@faa.gov. Before using any
approved AMOC on any airplane to which
the AMOC applies, notify your appropriate
principal inspector (PI) in the FAA Flight
Standards District Office (FSDO), or lacking
a PI, your local FSDO.
(2) Contacting the Manufacturer: For any
requirement in this AD to obtain corrective
actions from a manufacturer, the action must
be accomplished using a method approved
by the Manager, Small Airplane Standards
Branch, FAA; or the European Aviation
Safety Agency (EASA); or if there is a
delegated foreign airworthiness authority
Design Organization Approval (DOA). If
approved by the DOA, the approval must
include the DOA-authorized signature.
(h) Related Information
Refer to MCAI European Aviation Safety
Agency (EASA) AD No. 2017–0074, dated
April 28, 2017. You may examine the MCAI
on the Internet at https://
www.regulations.gov/document?D=FAA2017-0638-0002.
nlaroche on DSKBBV9HB2PROD with RULES
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(IBR) of the service information listed in this
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part 51.
(2) You must use this service information
as applicable to do the actions required by
this AD, unless this AD specifies otherwise.
(i) Diamond Aircraft Industries GmbH
Mandatory Service Bulletin MSB 42–126/
MSB 42NG–066, dated March 27, 2017
(single document).
(ii) Diamond Aircraft Industries GmbH
Work Instruction WI–MSB 42–126/WI–MSB
42NG–066, dated March 27, 2017 (single
document).
(3) For Diamond Aircraft Industries GmbH
service information identified in this AD,
contact Diamond Aircraft Industries GmbH,
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(4) You may view this service information
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VerDate Sep<11>2014
15:36 Sep 05, 2017
Jkt 241001
Issued in Kansas City, Missouri, on August
28, 2017.
Melvin Johnson,
Deputy Director, Policy and Innovation
Division, Aircraft Certification Service.
[FR Doc. 2017–18624 Filed 9–5–17; 8:45 am]
BILLING CODE 4910–13–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
21 CFR Part 112
[Docket No. FDA–2011–N–0921]
Standards for the Growing, Harvesting,
Packing, and Holding of Produce for
Human Consumption: What You Need
To Know About the Food and Drug
Administration Regulation; Small
Entity Compliance Guide; Availability
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Notification of availability.
The Food and Drug
Administration (FDA, the Agency, or
we) is announcing the availability of a
guidance for industry entitled
‘‘Standards for the Growing, Harvesting,
Packing, and Holding of Produce for
Human Consumption: What You Need
to Know About the FDA Regulation:
Small Entity Compliance Guide.’’ The
small entity compliance guide (SECG) is
intended to help small entities comply
with the final rule entitled ‘‘Standards
for the Growing, Harvesting, Packing,
and Holding of Produce for Human
Consumption.’’
SUMMARY:
The announcement of the
guidance is published in the Federal
Register on September 6, 2017.
ADDRESSES: You may submit either
electronic or written comments on
Agency guidances at any time as
follows:
DATES:
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
PO 00000
Frm 00011
Fmt 4700
Sfmt 4700
42031
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 Office, 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–
2011–N–0921 for ‘‘What You Need to
Know About the FDA Regulation:
Standards for the Growing, Harvesting,
Packing, and Holding of Produce for
Human Consumption—Small Entity
Compliance Guide.’’ Received
comments 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
Office between 9 a.m. and 4 p.m.,
Monday through Friday.
• Confidential Submissions—To
submit a comment with confidential
information that you do not wish to be
made publicly available, submit your
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
E:\FR\FM\06SER1.SGM
06SER1
42032
Federal Register / Vol. 82, No. 171 / Wednesday, September 6, 2017 / Rules and Regulations
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.gpo.gov/
fdsys/pkg/FR-2015-09-18/pdf/201523389.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.
See the SUPPLEMENTARY INFORMATION
section for electronic access to the
SECG.
FOR FURTHER INFORMATION CONTACT:
Samir Assar, Center for Food Safety and
Applied Nutrition, Food and Drug
Administration, 5001 Campus Dr.,
College Park, MD 20740, 240–402–1636.
SUPPLEMENTARY INFORMATION:
nlaroche on DSKBBV9HB2PROD with RULES
I. Background
In the Federal Register of November
27, 2015 (80 FR 74353), we issued a
final rule entitled ‘‘Standards for the
Growing, Harvesting, Packing, and
Holding of Produce for Human
Consumption’’ (the final rule) that
establishes science-based minimum
standards for the safe growing,
harvesting, packing, and holding of
produce, meaning fruits and vegetables
grown for human consumption. The
final rule, which is codified at 21 CFR
part 112, became effective January 26,
2016, but has staggered compliance
dates starting January 26, 2017.
We examined the economic
implications of the final rule as required
by the Regulatory Flexibility Act (5
U.S.C. 601–612) and determined that
the final rule will have a significant
economic impact on a substantial
number of small entities. In compliance
with section 212 of the Small Business
Regulatory Enforcement Fairness Act
(Pub. L. 104–121, as amended by Pub.
L. 110–28), we are making available the
SECG to reduce the burden of
determining how to comply by further
explaining and clarifying the actions
that a small entity must take to comply
with the rule.
We are issuing the SECG consistent
with our good guidance practices
VerDate Sep<11>2014
15:36 Sep 05, 2017
Jkt 241001
regulation (21 CFR 10.115(c)(2)). The
SECG represents the current thinking of
FDA on this topic. It does not establish
any rights for any person and is not
binding on FDA or the public. You can
use an alternative approach if it satisfies
the requirements of the applicable
statutes and regulations. This is not a
significant regulatory action subject to
Executive Order 12866 and does not
impose any additional burden on
regulated entities.
II. Paperwork Reduction Act of 1995
This guidance refers to previously
approved collections of information
found in FDA regulations. These
collections of information are subject to
review by the Office of Management and
Budget (OMB) under the Paperwork
Reduction Act of 1995 (44 U.S.C. 3501–
3520). The collections of information in
part 112 have been approved under
OMB control number 0910–0816.
III. Electronic Access
Persons with access to the Internet
may obtain the SECG at either https://
www.fda.gov/FoodGuidances, or https://
www.regulations.gov. Use the FDA Web
site listed in the previous sentence to
find the most current version of the
guidance.
Dated: August 30, 2017.
Anna K. Abram,
Deputy Commissioner for Policy, Planning,
Legislation, and Analysis.
[FR Doc. 2017–18811 Filed 9–5–17; 8:45 am]
BILLING CODE 4164–01–P
DEPARTMENT OF HOMELAND
SECURITY
Coast Guard
33 CFR Part 117
[Docket No. USCG–2017–0807]
Drawbridge Operation Regulation;
Newtown Creek, New York, NY
Coast Guard, DHS.
Notice of deviation from
drawbridge regulation.
AGENCY:
ACTION:
The Coast Guard has issued a
temporary deviation from the operating
schedule that governs the Pulaski Bridge
across Newtown Creek, mile 0.6 at New
York City, New York. This deviation is
necessary to facilitate planned repairs
and will allow the owner to temporarily
close the draw during weeknights for
periods not to exceed five hours.
DATES: This deviation is effective from
12:01 a.m. on September 19, 2017
through 5 a.m. on December 30, 2017.
SUMMARY:
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Sfmt 9990
The docket for this
deviation, USCG–2017–0807, is
available at https://www.regulations.gov.
Type the docket number in the
‘‘SEARCH’’ box and click ‘‘SEARCH’’.
Click on Open Docket Folder on the line
associated with this deviation.
FOR FURTHER INFORMATION CONTACT: If
you have questions on this temporary
deviation, call or email James M. Moore,
Bridge Management Specialist, First
District Bridge Branch, U.S. Coast
Guard; telephone 212–514–4334, email
James.M.Moore2@uscg.mil.
SUPPLEMENTARY INFORMATION: The owner
of the bridge, the New York City
Department of Transportation, requested
a temporary deviation in order to
facilitate planned repairs of the bridge
including replacement of the grease
piping system as well as installation of
new span lock shoes, steel shims and
horizontal/vertical bolts.
The Pulaski Bridge across Newtown
Creek, mile 0.6 at New York City, New
York is a double-leaf bascule bridge
with a vertical clearance of 39 feet at
mean high water and 43 feet at mean
low water in the closed position. The
existing drawbridge operating
regulations are listed at 33 CFR
117.801(g)(1)–(2).
The temporary deviation will allow
the Pulaski Bridge to remain closed each
Tuesday, Wednesday, Thursday, Friday
and Saturday from 12:01 a.m. to 5 a.m.
beginning September 19, 2017 until
December 30, 2017. The waterway is
transited by tug/barge traffic of various
sizes. Coordination with waterway users
has indicated no objections to the
proposed closure of the draw.
Vessels that can pass under the bridge
without an opening may do so at all
times. The bridge will not be able to
open for emergencies. There is no
alternate route for vessels to pass.
The Coast Guard will also inform the
users of the waterways through our
Local and Broadcast Notices to Mariners
of the change in operating schedule for
the bridge so vessel operators may
arrange their transits to minimize any
impact caused by the temporary
deviation.
In accordance with 33 CFR 117.35(e),
the drawbridge must return to its regular
operating schedule immediately at the
end of the effective period of this
temporary deviation. This deviation
from the operating regulations is
authorized under 33 CFR 117.35.
ADDRESSES:
Dated: August 31, 2017.
Christopher J. Bisignano,
Supervisory Bridge Management Specialist,
First Coast Guard District.
[FR Doc. 2017–18822 Filed 9–5–17; 8:45 am]
BILLING CODE 9110–04–P
E:\FR\FM\06SER1.SGM
06SER1
Agencies
[Federal Register Volume 82, Number 171 (Wednesday, September 6, 2017)]
[Rules and Regulations]
[Pages 42031-42032]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2017-18811]
=======================================================================
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
21 CFR Part 112
[Docket No. FDA-2011-N-0921]
Standards for the Growing, Harvesting, Packing, and Holding of
Produce for Human Consumption: What You Need To Know About the Food and
Drug Administration Regulation; Small Entity Compliance Guide;
Availability
AGENCY: Food and Drug Administration, HHS.
ACTION: Notification of availability.
-----------------------------------------------------------------------
SUMMARY: The Food and Drug Administration (FDA, the Agency, or we) is
announcing the availability of a guidance for industry entitled
``Standards for the Growing, Harvesting, Packing, and Holding of
Produce for Human Consumption: What You Need to Know About the FDA
Regulation: Small Entity Compliance Guide.'' The small entity
compliance guide (SECG) is intended to help small entities comply with
the final rule entitled ``Standards for the Growing, Harvesting,
Packing, and Holding of Produce for Human Consumption.''
DATES: The announcement of the guidance is published in the Federal
Register on September 6, 2017.
ADDRESSES: You may submit either electronic or written comments on
Agency guidances at any time as follows:
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 Office, 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-2011-N-0921 for ``What You Need to Know About the FDA Regulation:
Standards for the Growing, Harvesting, Packing, and Holding of Produce
for Human Consumption--Small Entity Compliance Guide.'' Received
comments 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 Office between 9
a.m. and 4 p.m., Monday through Friday.
Confidential Submissions--To submit a comment with
confidential information that you do not wish to be made publicly
available, submit your 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
[[Page 42032]]
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.gpo.gov/fdsys/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.
See the SUPPLEMENTARY INFORMATION section for electronic access to
the SECG.
FOR FURTHER INFORMATION CONTACT: Samir Assar, Center for Food Safety
and Applied Nutrition, Food and Drug Administration, 5001 Campus Dr.,
College Park, MD 20740, 240-402-1636.
SUPPLEMENTARY INFORMATION:
I. Background
In the Federal Register of November 27, 2015 (80 FR 74353), we
issued a final rule entitled ``Standards for the Growing, Harvesting,
Packing, and Holding of Produce for Human Consumption'' (the final
rule) that establishes science-based minimum standards for the safe
growing, harvesting, packing, and holding of produce, meaning fruits
and vegetables grown for human consumption. The final rule, which is
codified at 21 CFR part 112, became effective January 26, 2016, but has
staggered compliance dates starting January 26, 2017.
We examined the economic implications of the final rule as required
by the Regulatory Flexibility Act (5 U.S.C. 601-612) and determined
that the final rule will have a significant economic impact on a
substantial number of small entities. In compliance with section 212 of
the Small Business Regulatory Enforcement Fairness Act (Pub. L. 104-
121, as amended by Pub. L. 110-28), we are making available the SECG to
reduce the burden of determining how to comply by further explaining
and clarifying the actions that a small entity must take to comply with
the rule.
We are issuing the SECG consistent with our good guidance practices
regulation (21 CFR 10.115(c)(2)). The SECG represents the current
thinking of FDA on this topic. It does not establish any rights for any
person and is not binding on FDA or the public. You can use an
alternative approach if it satisfies the requirements of the applicable
statutes and regulations. This is not a significant regulatory action
subject to Executive Order 12866 and does not impose any additional
burden on regulated entities.
II. Paperwork Reduction Act of 1995
This guidance refers to previously approved collections of
information found in FDA regulations. These collections of information
are subject to review by the Office of Management and Budget (OMB)
under the Paperwork Reduction Act of 1995 (44 U.S.C. 3501-3520). The
collections of information in part 112 have been approved under OMB
control number 0910-0816.
III. Electronic Access
Persons with access to the Internet may obtain the SECG at either
https://www.fda.gov/FoodGuidances, or https://www.regulations.gov. Use
the FDA Web site listed in the previous sentence to find the most
current version of the guidance.
Dated: August 30, 2017.
Anna K. Abram,
Deputy Commissioner for Policy, Planning, Legislation, and Analysis.
[FR Doc. 2017-18811 Filed 9-5-17; 8:45 am]
BILLING CODE 4164-01-P