Occupational Safety and Health Investigations of Places of Employment, 19848-19849 [2014-07987]
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19848
Federal Register / Vol. 79, No. 69 / Thursday, April 10, 2014 / Proposed Rules
PART 39—AIRWORTHINESS
DIRECTIVES
1. The authority citation for part 39
continues to read as follows:
■
Authority: 49 U.S.C. 106(g), 40113, 44701.
§ 39.13
[Amended]
2. The FAA amends § 39.13 by adding
the following new airworthiness
directive (AD):
■
Airbus: Docket No. FAA–2014–0193;
Directorate Identifier 2013–NM–234–AD.
(a) Comments Due Date
We must receive comments by May 27,
2014.
(b) Affected ADs
None.
(c) Applicability
This AD applies to Airbus Model A318–
111, –112, –121, and –122 airplanes; Model
A319–111, –112, –113, –114, –115, –131,
–132, and –133 airplanes; Model A320–111,
–211, –212, –214, –231, –232, and –233
airplanes; and Model A321–111, –112, –131,
–211, –212, –213, –231, and –232 airplanes;
certificated in any category; all manufacturer
serial numbers on which Airbus modification
21202 has been embodied in production,
except those on which modification 152569
has been embodied in production.
(d) Subject
Air Transport Association (ATA) of
America Code 53, Fuselage.
(e) Reason
This AD was prompted by a report of a
crack found in the side box beam flange of
the fuselage at the frame (FR) 43 level during
a fatigue test campaign. We are issuing this
AD to prevent cracking in the side box beam
flange of the fuselage, which could affect the
structural integrity of the airplane.
ehiers on DSK2VPTVN1PROD with PROPOSALS-1
(f) Compliance
Comply with this AD within the
compliance times specified, unless already
done.
(g) Inspection
At the time specified in paragraph (g)(1) or
(g)(2) of this AD, whichever occurs later: Do
a rototest inspection for cracking of the beam
flange of the stiffener 15 side box on the leftand right-hand sides in the FR43 area, in
accordance with the Accomplishment
Instructions of Airbus Service Bulletin A320–
53–1258, dated October 18, 2012. Repeat the
inspection thereafter at intervals not to
exceed 7,500 flight cycles or 15, 000 flight
hours, whichever occurs first.
(1) Before exceeding 24,000 flight cycles or
48,000 flight hours, whichever occurs first
since the airplane’s first flight.
(2) Within 3,000 flight cycles or 6,000
flight hours, whichever occurs first after the
effective date of this AD.
(h) Corrective Action
If any crack is found during any inspection
required by paragraph (g) of this AD: Before
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15:10 Apr 09, 2014
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further flight, repair using a method
approved by the Manager, International
Branch, ANM–116, Transport Airplane
Directorate, FAA; or European Aviation
Safety Agency (EASA) (or its delegated agent,
or the Design Approval Holder (DAH) with
EASA design organization approval). For a
repair method to be approved, the repair
approval must specifically refer to this AD.
(i) Modification
Before exceeding 48,000 flight cycles or
96,000 flight hours, whichever occurs first
since the airplane’s first flight: Modify the
fittings on the left- and right-hand sides of
the torsion box, including doing all
applicable related investigative and
corrective actions, in accordance with the
Accomplishment Instructions of Airbus
Service Bulletin A320–53–1251, Revision 01,
dated October 18, 2013; except where Airbus
Service Bulletin A320–53–1251, Revision 01,
dated October 18, 2013, specifies to contact
Airbus for repair, before further flight, repair
using a method approved by the Manager,
International Branch, ANM–116, Transport
Airplane Directorate, FAA; or European
Aviation Safety Agency (EASA) (or its
delegated agent, or the Design Approval
Holder (DAH) with EASA design
organization approval). For a repair method
to be approved, the repair approval must
specifically refer to this AD.
(j) Terminating Action
Modification of the airplane as required by
paragraph (i) of this AD constitutes
terminating action for the repetitive
inspections required by paragraph (g) of this
AD.
(k) Credit for Previous Actions
This paragraph provides credit for actions
required by paragraph (i) of this AD, if those
actions were performed before the effective
date of this AD using Airbus Service Bulletin
A320–53–1251, November 16, 2012, which is
not incorporated by reference in this AD.
(l) Other FAA AD Provisions
The following provisions also apply to this
AD:
(1) Alternative Methods of Compliance
(AMOCs): The Manager, International
Branch, ANM–116, 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 International Branch, send it to ATTN:
Sanjay Ralhan, Aerospace Engineer,
International Branch, ANM 116, Transport
Airplane Directorate, FAA, 1601 Lind
Avenue SW., Renton, WA 98057–3356;
telephone (425) 227 1405; fax (425) 227–
1149. Information may be emailed to: 9ANM-116-AMOC-REQUESTS@faa.gov.
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. The AMOC
approval letter must specifically reference
this AD.
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Fmt 4702
Sfmt 4702
(2) Airworthy Product: For any requirement
in this AD to obtain corrective actions from
a manufacturer, use these actions if they are
FAA-approved. Corrective actions are
considered FAA-approved if they were
approved by the State of Design Authority (or
its delegated agent, or the DAH with a State
of Design Authority’s design organization
approval, as applicable). For a repair method
to be approved, the repair approval must
specifically refer to this AD. You are required
to ensure the product is airworthy before it
is returned to service.
(m) Related Information
(1) Refer to Mandatory Continuing
Airworthiness Information (MCAI) EASA
Airworthiness Directive 2013–0261, dated
October 28, 2013, for related information.
This MCAI may be found in the AD docket
on the Internet at https://www.regulations.gov
by searching for and locating it in Docket No.
FAA–2014–0193.
(2) For service information identified in
this AD, contact Airbus, Airworthiness
Office—EAS, 1 Rond Point Maurice Bellonte,
31707 Blagnac Cedex, France; telephone +33
5 61 93 36 96; fax +33 5 61 93 44 51; email
account.airworth-eas@airbus.com; Internet
https://www.airbus.com. You may view this
service information at the FAA, Transport
Airplane Directorate, 1601 Lind Avenue SW.,
Renton, WA. For information on the
availability of this material at the FAA, call
425–227–1221.
Issued in Renton, Washington, on April 1,
2014.
Michael Kaszycki,
Acting Manager, Transport Airplane
Directorate, Aircraft Certification Service.
[FR Doc. 2014–08071 Filed 4–9–14; 8:45 am]
BILLING CODE 4910–13–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
42 CFR Part 85a
[Docket No. CDC–2014–0001; NIOSH–271]
RIN 0920–AA51
Occupational Safety and Health
Investigations of Places of
Employment
Centers for Disease Control and
Prevention, HHS.
ACTION: Notice of proposed rulemaking;
withdrawal.
AGENCY:
The National Institute for
Occupational Safety and Health
(NIOSH) in the Centers for Disease
Control and Prevention (CDC) within
the Department of Health and Human
Services (HHS) is withdrawing a
previously published notice of proposed
rulemaking that solicited public
comment on minor technical
amendments to regulatory text.
DATES: The notice of proposed
rulemaking published at 79 FR 2809,
SUMMARY:
E:\FR\FM\10APP1.SGM
10APP1
Federal Register / Vol. 79, No. 69 / Thursday, April 10, 2014 / Proposed Rules
January 16, 2014, is withdrawn,
effective immediately.
FOR FURTHER INFORMATION CONTACT:
Teresa Schnorr Ph.D., Director NIOSH
Division of Surveillance, Hazard
Evaluations and Field Studies
(DSHEFS); 4676 Columbia Parkway,
Cincinnati, OH 45226; 513–841–4428
(this is not a toll-free number).
SUPPLEMENTARY INFORMATION: On
January 16, 2014, HHS published a
notice of proposed rulemaking (NPRM)
to make minor technical amendments to
the regulatory text in 42 CFR Part 85a
(79 FR 2809). On the same date, HHS
simultaneously published a companion
direct final rule (DFR) that offered
identical updates because the agency
believed that the revisions were noncontroversial and unlikely to generate
significant adverse comment (79 FR
2789). In the NPRM preamble, HHS
stated that if no significant adverse
comments were received by March 17,
2014, the NPRM would be withdrawn
and the effective date of the final rule
would be confirmed within 30 days of
the conclusion of the comment period.
HHS received one public comment that
was not a significant adverse comment,
but rather was in support of the
companion NPRM. Because HHS did
not receive any significant adverse
comments to the NPRM within the
specified comment period, we hereby
withdraw this NPRM from rulemaking.
Dated: April 3, 2014.
Kathleen Sebelius,
Secretary.
[FR Doc. 2014–07987 Filed 4–9–14; 8:45 am]
BILLING CODE 4163–18–P
FEDERAL COMMUNICATIONS
COMMISSION
47 CFR Part 76
[MB Docket No. 10–71; FCC 14–29]
Network Non-Duplication and
Syndicated Exclusivity Rules
Federal Communications
Commission.
ACTION: Proposed rule.
AGENCY:
In this document, the
Commission seeks comment on whether
to eliminate or modify the network nonduplication and syndicated exclusivity
rules in light of changes in the video
marketplace in the more than 40 years
since these rules were adopted. The
Commission seeks comment on whether
the exclusivity rules are still needed to
protect broadcasters’ ability to compete
in the video marketplace and to ensure
that program suppliers have sufficient
ehiers on DSK2VPTVN1PROD with PROPOSALS-1
SUMMARY:
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15:10 Apr 09, 2014
Jkt 232001
incentives to develop new and diverse
programming and on the impact of
eliminating of the exclusivity rules.
DATES: Comments for this proceeding
are due on or before May 12, 2014; reply
comments are due on or before June 9,
2014.
ADDRESSES: You may submit comments,
identified by MB Docket No. 10–71, by
any of the following methods:
• Federal Communications
Commission’s Web site: https://
fjallfoss.fcc.gov/ecfs2/. Follow the
instructions for submitting comments.
• Mail: Filings can be sent by hand or
messenger delivery, by commercial
overnight courier, or by first-class or
overnight U.S. Postal Service mail
(although the Commission continues to
experience delays in receiving U.S.
Postal Service mail). All filings must be
addressed to the Commission’s
Secretary, Office of the Secretary,
Federal Communications Commission.
• People With Disabilities: Contact
the FCC to request reasonable
accommodations (accessible format
documents, sign language interpreters,
CART, etc.) by email: FCC504@fcc.gov
or phone: (202) 418–0530 or TTY: (202)
418–0432.
For detailed instructions for submitting
comments and additional information
on the rulemaking process, see the
SUPPLEMENTARY INFORMATION section of
this document.
FOR FURTHER INFORMATION CONTACT: For
additional information, contact Kathy
Berthot, Kathy.Berthot@fcc.gov, of the
Media Bureau, Policy Division, (202)
418–7454.
SUPPLEMENTARY INFORMATION: This is a
summary of the Commission’s Further
Notice of Proposed Rulemaking, FCC
14–29, adopted on March 31, 2014 and
released on March 31, 2014. The full
text is available for public inspection
and copying during regular business
hours in the FCC Reference Center,
Federal Communications Commission,
445 12th Street SW., CY–A257,
Washington, DC 20554. This document
will also be available via ECFS (https://
www.fcc.gov/cgb/ecfs/). Documents will
be available electronically in ASCII,
Word 97, and/or Adobe Acrobat. The
complete text may be purchased from
the Commission’s copy contractor, 445
12th Street SW., Room CY–B402,
Washington, DC 20554. To request this
document in accessible formats
(computer diskettes, large print, audio
recording, and Braille), send an email to
fcc504@fcc.gov or call the Commission’s
Consumer and Governmental Affairs
Bureau at (202) 418–0530 (voice), (202)
418–0432 (TTY).
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19849
This document contains no proposed
information collection requirements.
SUMMARY:
I. Introduction
1. We are issuing this FNPRM to
solicit additional comment on whether
we should eliminate or modify our
network non-duplication and
syndicated exclusivity rules. We
received numerous comments on this
issue in response to the NPRM.
However, the record developed in this
proceeding to date is not sufficient for
us to yet make a determination whether
the exclusivity rules are still needed in
today’s competitive video marketplace
or to assess the potential impact on
affected parties of eliminating these
rules. Given the complex issues
involved, we believe it is necessary and
appropriate to undertake a more
comprehensive review of the exclusivity
rules and to compile a more complete
record.
II. Background
2. A broadcaster may carry network
and syndicated programming on its
local television station(s) only with the
permission of the networks or
syndicators that own or hold the rights
to that programming, as reflected in
network/affiliate agreements or
syndication agreements. In addition, the
ability of broadcasters to grant
retransmission consent for MVPD
carriage may be constrained by the
network/affiliate agreement or by the
syndication agreement because such
agreements generally limit the
geographical area in which the station
holds exclusive rights to network or
syndicated programming. The
Commission’s network non-duplication
and syndicated exclusivity rules are
designed to serve as a means of
enforcing contractual exclusivity
agreements entered into between
broadcasters, which purchase the
distribution rights to programming, and
networks and syndicators, which supply
the programming. Thus, the network
non-duplication and syndicated
exclusivity rules require that the
broadcaster have contractual exclusivity
rights and provide proper notice to the
relevant MVPD, requesting that an
MVPD delete duplicative network or
syndicated programming. The rules may
be invoked by stations that elect
retransmission consent in their local
markets, even if they are not actually
carried by the MVPD, to prevent an
MVPD from carrying programming of a
distant station that duplicates local
broadcast station programming. By
requiring MVPDs to delete duplicative
network or syndicated programming
E:\FR\FM\10APP1.SGM
10APP1
Agencies
[Federal Register Volume 79, Number 69 (Thursday, April 10, 2014)]
[Proposed Rules]
[Pages 19848-19849]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2014-07987]
=======================================================================
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
42 CFR Part 85a
[Docket No. CDC-2014-0001; NIOSH-271]
RIN 0920-AA51
Occupational Safety and Health Investigations of Places of
Employment
AGENCY: Centers for Disease Control and Prevention, HHS.
ACTION: Notice of proposed rulemaking; withdrawal.
-----------------------------------------------------------------------
SUMMARY: The National Institute for Occupational Safety and Health
(NIOSH) in the Centers for Disease Control and Prevention (CDC) within
the Department of Health and Human Services (HHS) is withdrawing a
previously published notice of proposed rulemaking that solicited
public comment on minor technical amendments to regulatory text.
DATES: The notice of proposed rulemaking published at 79 FR 2809,
[[Page 19849]]
January 16, 2014, is withdrawn, effective immediately.
FOR FURTHER INFORMATION CONTACT: Teresa Schnorr Ph.D., Director NIOSH
Division of Surveillance, Hazard Evaluations and Field Studies
(DSHEFS); 4676 Columbia Parkway, Cincinnati, OH 45226; 513-841-4428
(this is not a toll-free number).
SUPPLEMENTARY INFORMATION: On January 16, 2014, HHS published a notice
of proposed rulemaking (NPRM) to make minor technical amendments to the
regulatory text in 42 CFR Part 85a (79 FR 2809). On the same date, HHS
simultaneously published a companion direct final rule (DFR) that
offered identical updates because the agency believed that the
revisions were non-controversial and unlikely to generate significant
adverse comment (79 FR 2789). In the NPRM preamble, HHS stated that if
no significant adverse comments were received by March 17, 2014, the
NPRM would be withdrawn and the effective date of the final rule would
be confirmed within 30 days of the conclusion of the comment period.
HHS received one public comment that was not a significant adverse
comment, but rather was in support of the companion NPRM. Because HHS
did not receive any significant adverse comments to the NPRM within the
specified comment period, we hereby withdraw this NPRM from rulemaking.
Dated: April 3, 2014.
Kathleen Sebelius,
Secretary.
[FR Doc. 2014-07987 Filed 4-9-14; 8:45 am]
BILLING CODE 4163-18-P