Produce Safety Rule: Enforcement Policy for Entities Growing, Harvesting, Packing, or Holding Hops, Wine Grapes, Pulse Crops, and Almonds; Guidance for Industry; Availability, 11644-11646 [2019-05953]
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Federal Register / Vol. 84, No. 60 / Thursday, March 28, 2019 / Rules and Regulations
(2) For diffuser cases with a rear outer
flange that have fewer than 20,000 CSN on
the effective date of this AD, perform an
initial BSI of zones 1, 2, and 3 of the diffuser
case M-flange within 21,300 CSN, in
accordance with the Accomplishment
Instructions, paragraphs 2.A. through 2.G. for
the appropriate engine model, of IAE Alert
NMSB V2500–ENG–72–A0706, dated
February 14, 2019.
(3) If no cracks are found, perform a
repetitive BSI not to exceed every 2,100
cycles since the previous BSI.
(4) If cracks are found, remove the diffuser
case and replace with a part eligible for
installation or repeat the BSI within the
intervals in either Table 2: Fly on Limits or
Table 4: Fly on Limits, as appropriate for the
affected the engine model, of IAE Alert
NMSB V2500–ENG–72–A0706, dated
February 14, 2019.
(h) Credit for Previous Actions
You may take credit for the actions that are
required by paragraph (g)(1) and (2) of this
AD, if you performed those actions before the
effective date of this AD using IAE V2500
Special Instruction (SI) No. 350F–18, Rev. 1,
dated December 17, 2018; IAE V2500 SI No.
356F–18, Rev. 1, dated January 9, 2019; IAE
V2500 SI No. 372F–18, dated January 8,
2019; or IAE V2500 Special SI No. 04F–19,
dated January 14, 2019.
amozie on DSK9F9SC42PROD with RULES
(i) Alternative Methods of Compliance
(AMOCs)
(1) The Manager, ECO branch, FAA, has
the authority to approve AMOCs for this AD,
if requested using the procedures found in 14
CFR 39.19. In accordance with 14 CFR 39.19,
send your request to your principal inspector
or local Flight Standards District Office, as
appropriate. If sending information directly
to the manager of the certification office,
send it to the attention of the person
identified in paragraph (j) of this AD. You
may email your request to: ANE-AD-AMOC@
faa.gov.
(2) Before using any approved AMOC,
notify your appropriate principal inspector,
or lacking a principal inspector, the manager
of the local flight standards district office/
certificate holding district office.
VerDate Sep<11>2014
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(j) Related Information
For more information about this AD,
contact Barbara Caufield, Aerospace
Engineer, ECO Branch, FAA, 1200 District
Avenue, Burlington, MA 01803; phone: 781–
238–7146; fax: 781–238–7199; email:
barbara.caufield@faa.gov.
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
21 CFR Part 112
[Docket No. FDA–2019–D–1266]
(k) Material Incorporated by Reference
(1) The Director of the Federal Register
approved the incorporation by reference
(IBR) of the service information listed in this
paragraph under 5 U.S.C. 552(a) and 1 CFR
part 51.
(2) You must use this service information
as applicable to do the actions required by
this AD, unless the AD specifies otherwise.
(i) International Aero Engines (IAE) Alert
Non-Modification Service Bulletin V2500–
ENG–72–A0706, dated February 14, 2019.
(ii) [Reserved]
(3) For IAE service information identified
in this AD, contact International Aero
Engines AG, 400 Main Street, East Hartford,
CT, 06118; phone: 800–565–0140; email:
help24@pw.utc.com; internet: https://
fleetcare.pw.utc.com.
(4) You may view this service information
at FAA, Engine & Propeller Standards
Branch, 1200 District Avenue, Burlington,
MA 01803. For information on the
availability of this material at the FAA, call
781–238–7759.
(5) You may view this service information
that is incorporated by reference at the
National Archives and Records
Administration (NARA). For information on
the availability of this material at NARA, call
202–741–6030, or go to: https://
www.archives.gov/federal-register/cfr/ibrlocations.html.
Issued in Burlington, Massachusetts, on
March 22, 2019.
Karen M. Grant,
Acting Manager, Engine and Propeller
Standards Branch, Aircraft Certification
Service.
[FR Doc. 2019–05885 Filed 3–27–19; 8:45 am]
BILLING CODE 4910–13–P
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Produce Safety Rule: Enforcement
Policy for Entities Growing,
Harvesting, Packing, or Holding Hops,
Wine Grapes, Pulse Crops, and
Almonds; Guidance for Industry;
Availability
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Notification of availability.
The Food and Drug
Administration (FDA or we) is
announcing the availability of an
immediately in effect guidance for
industry entitled ‘‘Produce Safety Rule:
Enforcement Policy for Entities
Growing, Harvesting, Packing, or
Holding Hops, Wine Grapes, Pulse
Crops, and Almonds.’’ This document
states the intent of FDA to exercise
enforcement discretion regarding the
requirements of the ‘‘Standards for the
Growing, Harvesting, Packing, and
Holding of Produce for Human
Consumption’’ regulation (Produce
Safety Regulation) as they apply to
entities growing, harvesting, packing,
and holding hops, wine grapes, pulse
crops, and almonds.
DATES: The announcement of the
guidance is published in the Federal
Register on March 28, 2019.
ADDRESSES: You may submit either
electronic or written comments on
Agency guidances at any time as
follows:
SUMMARY:
Electronic Submissions
Submit electronic comments in the
following way:
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ER28MR19.000
11644
Federal Register / Vol. 84, No. 60 / Thursday, March 28, 2019 / Rules and Regulations
amozie on DSK9F9SC42PROD with RULES
• 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–
2019–D–1266 for ‘‘Produce Safety Rule:
Enforcement Policy for Entities
Growing, Harvesting, Packing, or
Holding Hops, Wine Grapes, Pulse
Crops, and Almonds: Guidance for
Industry.’’ 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 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
VerDate Sep<11>2014
16:25 Mar 27, 2019
Jkt 247001
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.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.
You may submit comments on any
guidance at any time (see 21 CFR
10.115(g)(5)).
Submit written requests for single
copies of the guidance to the Center for
Food Safety and Applied Nutrition,
Food and Drug Administration, 5001
Campus Dr., College Park, MD 20740.
Send two self-addressed adhesive labels
to assist that office in processing your
request. See the SUPPLEMENTARY
INFORMATION section for electronic
access to the guidance.
FOR FURTHER INFORMATION CONTACT:
Fazila Shakir, Center for Food Safety
and Applied Nutrition, Food and Drug
Administration, 5001 Campus Dr.,
College Park, MD 20740, 240–402–1355.
SUPPLEMENTARY INFORMATION:
I. Background
FDA is announcing the availability of
a guidance for industry entitled
‘‘Produce Safety Rule: Enforcement
Policy for Entities Growing, Harvesting,
Packing, or Holding Hops, Wine Grapes,
Pulse Crops, and Almonds.’’ We are
issuing the guidance consistent with our
good guidance practices regulation (21
CFR 10.115). The guidance represents
the current thinking of FDA on this
PO 00000
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Fmt 4700
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11645
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. In accordance with
§ 10.115(g)(2), we are implementing the
guidance immediately because we have
determined that prior public
participation is not feasible or
appropriate. Although the guidance
document is immediately in effect, FDA
will accept comments at any time. The
guidance is not subject to Executive
Order 12866.
The FDA Food Safety Modernization
Act (Pub. L. 111–353) directs FDA to
better protect public health by, among
other things, adopting a modern,
preventive, and risk-based approach to
food safety. The Produce Safety
Regulation is a set of science-based
minimum standards for the safe
growing, harvesting, packing, and
holding of fruits and vegetables grown
for human consumption. Produce is
subject to the Produce Safety Regulation
unless it is ‘‘not covered’’ or is eligible
for an exemption. Produce that is not
covered by the Produce Safety
Regulation includes that which is rarely
consumed raw (21 CFR 112.2(a)(1)),
produced for personal or on-farm
consumption (21 CFR 112.2(a)(2)), or
not a raw agricultural commodity (21
CFR 112.2(a)(3)).
Following the publication of the final
rule establishing the Produce Safety
Regulation, FDA received feedback from
some stakeholders that certain covered
commodities—hops, wine grapes, pulse
crops, and almonds—should be exempt
from the requirements of the Produce
Safety Regulation. After conducting an
initial review of how hops, wine grapes,
pulse crops, and almonds are grown,
harvested, packed, held, and used, FDA
has decided to exercise enforcement
discretion with respect to the Produce
Safety Regulation for entities growing,
harvesting, packing, or holding those
commodities while we consider
pursuing rulemaking to address the
unique circumstances they each present.
This means that we will not expect
entities growing, harvesting, packing, or
holding these commodities to meet any
of the Produce Safety Regulation
requirements with respect to these
commodities.
We will consider revising our intent
to exercise enforcement discretion if, for
example, new information becomes
available regarding safety concerns
associated with the production and
consumption of these commodities.
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Federal Register / Vol. 84, No. 60 / Thursday, March 28, 2019 / Rules and Regulations
II. Electronic Access
Persons with access to the internet
may obtain the guidance at either
https://www.fda.gov/FoodGuidances or
https://www.regulations.gov. Use the
FDA website listed in the previous
sentence to find the most current
version of the guidance.
Dated: March 22, 2019.
Lowell J. Schiller,
Acting Associate Commissioner for Policy.
[FR Doc. 2019–05953 Filed 3–27–19; 8:45 am]
BILLING CODE 4164–01–P
ENVIRONMENTAL PROTECTION
AGENCY
40 CFR Part 52
[EPA–R08–OAR–2018–0026; FRL–9991–25–
Region 8]
Approval and Promulgation of Air
Quality Implementation Plans; North
Dakota; Revisions to Air Pollution
Control Rules
Environmental Protection
Agency (EPA).
ACTION: Final rule.
AGENCY:
The Environmental Protection
Agency (EPA) is approving State
Implementation Plan (SIP) revisions
submitted by the State of North Dakota
on January 28, 2013, and November 11,
2016. The revisions include
amendments to North Dakota’s general
provisions, permit to construct,
prevention of significant deterioration
(PSD) of air quality, oil and gas, and fee
regulations. In addition, amendments to
the permit program include the
regulation of hazardous air pollutants
(HAPs), which may be regulated under
section 112 of the Clean Air Act (CAA).
Thus, the EPA is taking this action
pursuant to sections 110 and 112 of the
CAA.
DATES: This rule is effective on April 29,
2019.
ADDRESSES: The EPA has established a
docket for this action under Docket ID
No. EPA–R08–OAR–2018–0026. All
documents in the docket are listed on
the https://www.regulations.gov website.
Although listed in the index, some
information is not publicly available,
e.g., CBI or other information whose
disclosure is restricted by statute.
Certain other material, such as
copyrighted material, is not placed on
the internet and will be publicly
available only in hard copy form.
Publicly available docket materials are
available through https://
www.regulations.gov, or please contact
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SUMMARY:
VerDate Sep<11>2014
16:25 Mar 27, 2019
Jkt 247001
the person identified in the FOR FURTHER
section for
additional availability information.
FOR FURTHER INFORMATION CONTACT:
Jaslyn Dobrahner, Air Program, U.S.
Environmental Protection Agency
(EPA), Region 8, Mail Code 8P–AR,
1595 Wynkoop Street, Denver, Colorado
80202–1129, (303) 312–6252,
dobrahner.jaslyn@epa.gov.
SUPPLEMENTARY INFORMATION:
INFORMATION CONTACT
I. Background
In our notice of proposed rulemaking
published on May 14, 2018 (83 FR
22227), the EPA proposed to approve
revisions to North Dakota’s Air
Pollution Control Rules submitted by
the State of North Dakota on January 28,
2013, and November 11, 2016. In this
rulemaking, we are taking final action to
approve various revisions, including: To
add a general permit to construct
provision,1 update the definition of
‘‘volatile organic compounds’’ and PSD
rules; revise permit to construct and
PSD public participation methods;
clarify applicability of oil and gas
regulations; increase the application and
processing fees; add a significant
emission rate for greenhouse gas carbon
dioxide equivalent; add a definition of
‘‘actively producing’’ oil and gas wells;
remove greenhouse gas provisions
relating to the determination of a major
source and major modification; remove
the expired exemption of greenhouse
gases from biogenic sources; and
streamline a provision related to oil and
gas registration and reporting. The
North Dakota State Health Council
adopted the amendments on August 14,
2012, (effective January 1, 2013) and
February 24, 2016, (effective July 1,
2016) for the January 28, 2013, and
November 11, 2016, submittals,
respectively. The reasons for our
1 North Dakota Air Pollution Control (NDAC) rule
33–15–14–02.1.c reads in its entirety as follows,
‘‘General permits. The department may issue a
general permit to construct covering numerous
similar sources which are not subject to permitting
requirements under chapter 33.1–15–13 or 33.1–15–
15 or subpart B of section 33.1–15–22–03. Any
general permit shall comply with all requirements
applicable to other permits to construct and shall
identify criteria by which sources may qualify for
the general permit. A proposed general permit, any
changes to a general permit, and any renewal of a
general permit is subject to public comment. The
public comment procedures under subdivision b of
subsection 6 shall be used. To sources that qualify,
the department shall grant the conditions and terms
of the general permit. Sources that would qualify
for a general permit must apply to the department
for coverage under the terms of the general permit
or apply for an individual permit to construct.
Without repeating the public participation
procedures under subdivision b of subsection 6, the
department may grant a source’s request for
authorization to construct under the general
permit.’’
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approval are provided in detail in the
proposed rule. Additional reasons for
our approval of some provisions are
provided below in response to public
comments received on those topics.
II. Response to Comments
We received two comment letters
during the public comment period.
After reviewing the comments, the EPA
determined that the comments in the
first letter are outside the scope of our
proposed action and fail to identify any
material issue necessitating a response.
The remaining comments in the second
letter were jointly submitted by the
Sierra Club, Center for Biological
Diversity, and the National Parks
Conservation Association. Below is a
summary of the comments and the
EPA’s responses.
Comment: In general, the commenters
assert that the concept of a general
construction permit is not consistent
with the requirements of Section
110(a)(2)(C) of the CAA or 40 CFR
51.160—51.164 due to the nature of how
general permits are established and how
sources request coverage under general
permits.
Response: We disagree with the
commenters’ assertion that the concept
of a general construction permit is not
consistent with the requirements of
Section 110(a)(2)(C) of the CAA
(requirement that the state SIP contain
a program for enforcement of control
measures), and 40 CFR 51.160–51.164
(the EPA’s regulations relating, in part,
to minor source construction). The
State’s source-specific minor source
construction permit program was
originally approved as meeting the
criteria currently in 40 CFR 51.160–
51.163 on May 26, 1977, (42 FR 26977)
and as meeting the criteria in 40 CFR
51.164 on November 14, 1988, (53 FR
45763). The North Dakota’s SIPapproved minor source construction
permit program and other permitting
rules are codified at North Dakota Air
Pollution Control (NDAC) 33–15–14,
Designated Air Contaminant Sources
Permit to Construct Minor Source
Permit to Operate, Title V Permit to
Operate.
North Dakota’s general permit rule
requires that ‘‘[a]ny general permit shall
comply with all requirements applicable
to other permits to construct.’’
Therefore, a general permit would be
issued in accordance with essentially
the same State rules that apply to
sources seeking source-specific permits.
The general permit to construct
provision specifically excludes major
sources subject to permitting
requirements under chapter 33–15–13
(Emission Standards for Hazardous Air
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Agencies
[Federal Register Volume 84, Number 60 (Thursday, March 28, 2019)]
[Rules and Regulations]
[Pages 11644-11646]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2019-05953]
=======================================================================
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
21 CFR Part 112
[Docket No. FDA-2019-D-1266]
Produce Safety Rule: Enforcement Policy for Entities Growing,
Harvesting, Packing, or Holding Hops, Wine Grapes, Pulse Crops, and
Almonds; Guidance for Industry; Availability
AGENCY: Food and Drug Administration, HHS.
ACTION: Notification of availability.
-----------------------------------------------------------------------
SUMMARY: The Food and Drug Administration (FDA or we) is announcing the
availability of an immediately in effect guidance for industry entitled
``Produce Safety Rule: Enforcement Policy for Entities Growing,
Harvesting, Packing, or Holding Hops, Wine Grapes, Pulse Crops, and
Almonds.'' This document states the intent of FDA to exercise
enforcement discretion regarding the requirements of the ``Standards
for the Growing, Harvesting, Packing, and Holding of Produce for Human
Consumption'' regulation (Produce Safety Regulation) as they apply to
entities growing, harvesting, packing, and holding hops, wine grapes,
pulse crops, and almonds.
DATES: The announcement of the guidance is published in the Federal
Register on March 28, 2019.
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:
[[Page 11645]]
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-2019-D-1266 for ``Produce Safety Rule: Enforcement Policy for
Entities Growing, Harvesting, Packing, or Holding Hops, Wine Grapes,
Pulse Crops, and Almonds: Guidance for Industry.'' 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 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 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.
You may submit comments on any guidance at any time (see 21 CFR
10.115(g)(5)).
Submit written requests for single copies of the guidance to the
Center for Food Safety and Applied Nutrition, Food and Drug
Administration, 5001 Campus Dr., College Park, MD 20740. Send two self-
addressed adhesive labels to assist that office in processing your
request. See the SUPPLEMENTARY INFORMATION section for electronic
access to the guidance.
FOR FURTHER INFORMATION CONTACT: Fazila Shakir, Center for Food Safety
and Applied Nutrition, Food and Drug Administration, 5001 Campus Dr.,
College Park, MD 20740, 240-402-1355.
SUPPLEMENTARY INFORMATION:
I. Background
FDA is announcing the availability of a guidance for industry
entitled ``Produce Safety Rule: Enforcement Policy for Entities
Growing, Harvesting, Packing, or Holding Hops, Wine Grapes, Pulse
Crops, and Almonds.'' We are issuing the guidance consistent with our
good guidance practices regulation (21 CFR 10.115). The guidance
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. In accordance
with Sec. 10.115(g)(2), we are implementing the guidance immediately
because we have determined that prior public participation is not
feasible or appropriate. Although the guidance document is immediately
in effect, FDA will accept comments at any time. The guidance is not
subject to Executive Order 12866.
The FDA Food Safety Modernization Act (Pub. L. 111-353) directs FDA
to better protect public health by, among other things, adopting a
modern, preventive, and risk-based approach to food safety. The Produce
Safety Regulation is a set of science-based minimum standards for the
safe growing, harvesting, packing, and holding of fruits and vegetables
grown for human consumption. Produce is subject to the Produce Safety
Regulation unless it is ``not covered'' or is eligible for an
exemption. Produce that is not covered by the Produce Safety Regulation
includes that which is rarely consumed raw (21 CFR 112.2(a)(1)),
produced for personal or on-farm consumption (21 CFR 112.2(a)(2)), or
not a raw agricultural commodity (21 CFR 112.2(a)(3)).
Following the publication of the final rule establishing the
Produce Safety Regulation, FDA received feedback from some stakeholders
that certain covered commodities--hops, wine grapes, pulse crops, and
almonds--should be exempt from the requirements of the Produce Safety
Regulation. After conducting an initial review of how hops, wine
grapes, pulse crops, and almonds are grown, harvested, packed, held,
and used, FDA has decided to exercise enforcement discretion with
respect to the Produce Safety Regulation for entities growing,
harvesting, packing, or holding those commodities while we consider
pursuing rulemaking to address the unique circumstances they each
present. This means that we will not expect entities growing,
harvesting, packing, or holding these commodities to meet any of the
Produce Safety Regulation requirements with respect to these
commodities.
We will consider revising our intent to exercise enforcement
discretion if, for example, new information becomes available regarding
safety concerns associated with the production and consumption of these
commodities.
[[Page 11646]]
II. Electronic Access
Persons with access to the internet may obtain the guidance at
either https://www.fda.gov/FoodGuidances or https://www.regulations.gov. Use the FDA website listed in the previous
sentence to find the most current version of the guidance.
Dated: March 22, 2019.
Lowell J. Schiller,
Acting Associate Commissioner for Policy.
[FR Doc. 2019-05953 Filed 3-27-19; 8:45 am]
BILLING CODE 4164-01-P