Information Collection; Report of Shipment, 39052-39053 [2016-14119]
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ehiers on DSK5VPTVN1PROD with NOTICES
39052
Federal Register / Vol. 81, No. 115 / Wednesday, June 15, 2016 / Notices
ensuring Sabal Trail’s ability to
negotiate additional Transco
expansions. First, the proposed Order
incorporates the capacity lease
agreement between Transco and Sabal
Trail, which reflects terms Transco and
Sabal Trail reached when an
independent and motivated commercial
partner owned Transco. The proposed
Order gives Sabal Trail additional
flexibility and optionality in obtaining
the phased capacity expansions already
contemplated by the capacity lease
agreement. The proposed Order
terminates twelve years after it issues, in
order to cover the entirety of ETE’s
obligations for the expansions currently
outlined in the capacity lease
agreement.
Second, the Order requires that,
within one year of the closing of the
Acquisition, ETE offer to amend the
capacity lease agreement to allow Sabal
Trail to request expansions for as long
as an additional eight years after the last
expansion currently in the capacity
lease agreement. These provisions
ensure that Sabal Trail has the same
future expansion opportunities as
would have existed if an independent
Williams continued to own Transco.
ETE must offer future expansions on
the same terms and conditions that
Transco negotiated as an independent
entity. For each requested expansion,
ETE must inform Sabal Trail of the
estimated expansion cost, using the
same methodology for each that Transco
uses in its normal course of business.
ETE then is obligated to expand Transco
as requested by Sabal Trail. However, to
prevent Sabal Trail from requesting
cost-prohibitive expansions—
expansions that an independent
Williams would not have agreed to—
ETE retains the right to require Sabal
Trail to pay for the capital costs of the
expansion, in which case ETE would
not charge Sabal Trail a lease fee for that
particular expanded capacity.
The proposed Order does not obligate
ETE to expand Transco if Sabal Trail
does not have (or has not secured preconstruction commitments from
shippers for) sufficient capacity to use
the expansion to serve Florida. The
Acquisition does not change the
incentives of Transco’s owner to deny
capacity expansions to serve areas
outside of Florida. Thus, without this
limitation, the proposed Order could
give Sabal Trail expansion rights it
would have been unable to negotiate
from an independent Transco.
The Commission does not intend this
analysis to constitute an official
interpretation of the proposed Order or
to modify its terms in any way.
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By direction of the Commission.
Donald S. Clark,
Secretary.
[FR Doc. 2016–14092 Filed 6–14–16; 8:45 am]
BILLING CODE 6750–01–P
DEPARTMENT OF DEFENSE
GENERAL SERVICES
ADMINISTRATION
NATIONAL AERONAUTICS AND
SPACE ADMINISTRATION
[OMB Control No. 9000–0056; Docket 2016–
0053; Sequence 23]
Information Collection; Report of
Shipment
Department of Defense (DOD),
General Services Administration (GSA),
and National Aeronautics and Space
Administration (NASA).
ACTION: Notice of request for public
comments regarding an extension of an
existing OMB clearance.
AGENCY:
Under the provisions of the
Paperwork Reduction Act, the
Regulatory Secretariat Division will be
submitting to the Office of Management
and Budget (OMB) a request to review
and approve an extension of a
previously approved information
collection requirement concerning
report of shipment.
DATES: Submit comments on or before
August 15, 2016.
ADDRESSES: Submit comments
identified by Information Collection
9000–0056, Report of Shipment, by any
of the following methods:
• Regulations.gov: https://
www.regulations.gov.
Submit comments via the Federal
eRulemaking portal by searching the
OMB control number. Select the link
‘‘Submit a Comment’’ that corresponds
with ‘‘Information Collection 9000–
0056, Report of Shipment’’. Follow the
instructions provided at the ‘‘Submit a
Comment’’ screen. Please include your
name, company name (if any), and
‘‘Information Collection 9000–0056,
Report of Shipment’’ on your attached
document.
• Mail: General Services
Administration, Regulatory Secretariat
Division (MVCB), 1800 F Street NW.,
Washington, DC 20405. ATTN: Ms.
Flowers/IC 9000–0056, Report of
Shipment.
Instructions: Please submit comments
only and cite Information Collection
9000–0056, Report of Shipment, in all
correspondence related to this
collection. Comments received generally
SUMMARY:
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will be posted without change to https://
www.regulations.gov, including any
personal and/or business confidential
information provided. To confirm
receipt of your comment(s), please
check www.regulations.gov,
approximately two to three days after
submission to verify posting (except
allow 30 days for posting of comments
submitted by mail).
FOR FURTHER INFORMATION CONTACT: Mr.
Curtis E. Glover, Sr., Procurement
Analyst, Office of Acquisition Policy, by
telephone at 202–501–1448 or
curtis.glover@gsa.gov.
SUPPLEMENTARY INFORMATION:
A. Purpose
Per FAR 47.208, military (and, as
required, civilian agency) storage and
distribution points, depots, and other
receiving activities require advance
notice of shipments en-route from
contractors’ plants. Generally, this
notification is required only for
classified material; sensitive, controlled,
and certain other protected material;
explosives, and some other hazardous
materials; selected shipments requiring
movement control; or minimum carload
or truckload shipments. It facilitates
arrangements for transportation control,
labor, space, and use of materials
handling equipment at destination.
Also, timely receipt of notices by the
consignee transportation office
precludes the incurring of demurrage
and vehicle detention charges. Unless
otherwise directed by a contracting
officer, a contractor shall send the
notice to the consignee transportation
office at least twenty-four hours before
the arrival of the shipment.
B. Annual Reporting Burden
Respondents: 33.
Responses per Respondent: 303.
Annual Responses: 9,999.
Hours per Response: .167.
Total Burden Hours: 1,670.
C. Public Comments
Public comments are particularly
invited on: Whether this collection of
information is necessary; whether it will
have practical utility; whether our
estimate of the public burden of this
collection of information is accurate,
and based on valid assumptions and
methodology; ways to enhance the
quality, utility, and clarity of the
information to be collected; and ways in
which we can minimize the burden of
the collection of information on those
who are to respond, through the use of
appropriate technological collection
techniques or other forms of information
technology.
E:\FR\FM\15JNN1.SGM
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Federal Register / Vol. 81, No. 115 / Wednesday, June 15, 2016 / Notices
Obtaining Copies of Proposals:
Requesters may obtain a copy of the
information collection documents from
the General Services Administration,
Regulatory Secretariat Division (MVCB),
1800 F Street, Washington, DC 20405,
telephone 202–501–4755. Please cite
OMB Control No. 9000–0056, Report of
Shipment, in all correspondence.
Dated: June 9, 2016.
Lorin S. Curit,
Director, Federal Acquisition Policy Division,
Office of Governmentwide Acquisition Policy,
Office of Acquisition Policy, Office of
Governmentwide Policy.
[FR Doc. 2016–14119 Filed 6–14–16; 8:45 am]
BILLING CODE 6820–EP–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2012–N–0853]
Tobacco Product Manufacturing
Facility Visits
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Notice.
The Food and Drug
Administration (FDA), Center for
Tobacco Products (CTP) is announcing
an invitation for participation in its
Tobacco Product Manufacturing Facility
Visits. This program is intended to give
FDA staff an opportunity to visit
facilities involved in the manufacturing
of newly deemed tobacco products and
their components and parts, including
any related laboratory testing, and to
observe the manufacturing operations of
the tobacco industry. The purpose of
this document is to invite parties
interested in participating in Tobacco
Product Manufacturing Facility Visits to
submit requests to CTP.
DATES: Submit either an electronic or
written request for participation by
August 15, 2016. See section IV of this
document for information on requests
for participation.
ADDRESSES: If your facility is interested
in participating in Tobacco Product
Manufacturing Facility Visits, please
submit a request either electronically to
https://www.regulations.gov or in writing
to the Division of Dockets Management
(HFA–305), Food and Drug
Administration, 5630 Fishers Lane, Rm.
1061, Rockville, MD 20852.
FOR FURTHER INFORMATION CONTACT:
Matthew Brenner, Center for Tobacco
Products, Food and Drug
Administration, Document Control
Center, Bldg. 71, Rm. G335, 10903 New
ehiers on DSK5VPTVN1PROD with NOTICES
SUMMARY:
VerDate Sep<11>2014
15:15 Jun 14, 2016
Jkt 238001
Hampshire Ave., Silver Spring, MD
20993–0002, 877–287–1373, email:
CTPRegulations@fda.hhs.gov.
SUPPLEMENTARY INFORMATION:
I. Background
On June 22, 2009, the Family
Smoking Prevention and Tobacco
Control Act (Pub. L. 111–31; 123 Stat.
1776) was signed into law, amending
the Federal Food, Drug, and Cosmetic
Act (the FD&C Act) and giving FDA
authority to regulate tobacco product
manufacturing, distribution, and
marketing. The new provisions include,
among other things, the authority to
issue regulations related to tobacco
product manufacturing practice in order
to protect the public health and to
assure that tobacco products are in
compliance with the FD&C Act.
Specifically, section 906(e) of the FD&C
Act (21 U.S.C. 387f(e)) provides that in
applying manufacturing restrictions to
tobacco, the Secretary shall prescribe
regulations (which may differ based on
the type of tobacco product involved)
requiring that the methods used in, and
the facilities and controls used for, the
manufacture, preproduction design
validation (including a process to assess
the performance of a tobacco product),
packing, and storage of a tobacco
product conform to current good
manufacturing practice, or hazard
analysis and critical control point
methodology.
CTP is instituting Tobacco Product
Manufacturing Facility Visits to provide
FDA staff with the opportunity to:
• Observe tobacco product
manufacturing operations—from the
receipt of raw materials to the
distribution of newly deemed tobacco
products, and
• Learn about the manufacturing
practices and processes unique to your
facility and newly deemed tobacco
products.
This program will also inform FDA
staff as they implement the tobacco
provisions of the FD&C Act.
II. Description of the Tobacco Product
Manufacturing Facility Visits
In this program, groups of FDA staff
plan to observe the following facilities
and their operations:
• Manufacturing facilities, including
establishments that process, package,
label, and distribute different types of
newly deemed tobacco products (e.g.,
dissolvable products, gels, cigars, pipe
tobacco, waterpipe tobacco products,
and electronic nicotine delivery systems
(ENDS) (including e-cigarettes, ehookah, e-cigars, vape pens, advanced
refillable personal vaporizers, and
electronic pipes) and liquid nicotine
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39053
and flavors) (see 81 FR 28973, May 10,
2016),
• Laboratory facilities that perform
tobacco testing (whether third-party or
in-house), and
• Manufacturing facilities for tobacco
products for further manufacturing into
finished tobacco products (including,
but not limited to, components, parts,
flavors, casings, e-liquids).
Please note that Tobacco Product
Manufacturing Facility Visits are not
intended to include or replace official
FDA inspections of facilities to
determine compliance with the FD&C
Act; rather, these facility visits are
meant to educate FDA staff and improve
their understanding of the tobacco
industry and its manufacturing
operations.
III. Site Selection
CTP plans to select sites from one or
more of each of the following categories:
• Dissolvable products,
• Gels,
• Cigars,
• Pipe tobacco,
• Waterpipe tobacco products,
• ENDS (including e-cigarettes, ehookah, e-cigars, vape pens, advanced
refillable personal vaporizers, and
electronic pipes) and liquid nicotine
and flavors,
• Tobacco laboratories,
• Importers of finished tobacco
products,
• Distributors and wholesalers of
regulated tobacco products, and/or
• Manufacturers of tobacco products
for further manufacturing into finished
tobacco products (including, but not
limited to, components, parts, flavors,
casings, e-liquids).
Final site selections will be based on
the availability of CTP funds and
resources for the relevant fiscal year, as
well as the following factors, as
applicable: (1) Compliance status of the
requesting facility and affiliated firm; (2)
whether the requesting facility or
affiliated firm, if applicable, has a
significant request or marketing
application or submission pending with
FDA; and (3) whether the requesting
facility will be engaged in active
manufacturing or processing during the
proposed time of the visit. All travel
expenses associated with Tobacco
Product Manufacturer Facility Visits
will be the responsibility of CTP.
IV. Requests for Participation
The request for participation should
include the following identification
information:
• The name and contact information
(including address, phone number, and
email) of your point of contact for the
request;
E:\FR\FM\15JNN1.SGM
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Agencies
[Federal Register Volume 81, Number 115 (Wednesday, June 15, 2016)]
[Notices]
[Pages 39052-39053]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2016-14119]
=======================================================================
-----------------------------------------------------------------------
DEPARTMENT OF DEFENSE
GENERAL SERVICES ADMINISTRATION
NATIONAL AERONAUTICS AND SPACE ADMINISTRATION
[OMB Control No. 9000-0056; Docket 2016-0053; Sequence 23]
Information Collection; Report of Shipment
AGENCY: Department of Defense (DOD), General Services Administration
(GSA), and National Aeronautics and Space Administration (NASA).
ACTION: Notice of request for public comments regarding an extension of
an existing OMB clearance.
-----------------------------------------------------------------------
SUMMARY: Under the provisions of the Paperwork Reduction Act, the
Regulatory Secretariat Division will be submitting to the Office of
Management and Budget (OMB) a request to review and approve an
extension of a previously approved information collection requirement
concerning report of shipment.
DATES: Submit comments on or before August 15, 2016.
ADDRESSES: Submit comments identified by Information Collection 9000-
0056, Report of Shipment, by any of the following methods:
Regulations.gov: https://www.regulations.gov.
Submit comments via the Federal eRulemaking portal by searching the
OMB control number. Select the link ``Submit a Comment'' that
corresponds with ``Information Collection 9000-0056, Report of
Shipment''. Follow the instructions provided at the ``Submit a
Comment'' screen. Please include your name, company name (if any), and
``Information Collection 9000-0056, Report of Shipment'' on your
attached document.
Mail: General Services Administration, Regulatory
Secretariat Division (MVCB), 1800 F Street NW., Washington, DC 20405.
ATTN: Ms. Flowers/IC 9000-0056, Report of Shipment.
Instructions: Please submit comments only and cite Information
Collection 9000-0056, Report of Shipment, in all correspondence related
to this collection. Comments received generally will be posted without
change to https://www.regulations.gov, including any personal and/or
business confidential information provided. To confirm receipt of your
comment(s), please check www.regulations.gov, approximately two to
three days after submission to verify posting (except allow 30 days for
posting of comments submitted by mail).
FOR FURTHER INFORMATION CONTACT: Mr. Curtis E. Glover, Sr., Procurement
Analyst, Office of Acquisition Policy, by telephone at 202-501-1448 or
curtis.glover@gsa.gov.
SUPPLEMENTARY INFORMATION:
A. Purpose
Per FAR 47.208, military (and, as required, civilian agency)
storage and distribution points, depots, and other receiving activities
require advance notice of shipments en-route from contractors' plants.
Generally, this notification is required only for classified material;
sensitive, controlled, and certain other protected material;
explosives, and some other hazardous materials; selected shipments
requiring movement control; or minimum carload or truckload shipments.
It facilitates arrangements for transportation control, labor, space,
and use of materials handling equipment at destination. Also, timely
receipt of notices by the consignee transportation office precludes the
incurring of demurrage and vehicle detention charges. Unless otherwise
directed by a contracting officer, a contractor shall send the notice
to the consignee transportation office at least twenty-four hours
before the arrival of the shipment.
B. Annual Reporting Burden
Respondents: 33.
Responses per Respondent: 303.
Annual Responses: 9,999.
Hours per Response: .167.
Total Burden Hours: 1,670.
C. Public Comments
Public comments are particularly invited on: Whether this
collection of information is necessary; whether it will have practical
utility; whether our estimate of the public burden of this collection
of information is accurate, and based on valid assumptions and
methodology; ways to enhance the quality, utility, and clarity of the
information to be collected; and ways in which we can minimize the
burden of the collection of information on those who are to respond,
through the use of appropriate technological collection techniques or
other forms of information technology.
[[Page 39053]]
Obtaining Copies of Proposals: Requesters may obtain a copy of the
information collection documents from the General Services
Administration, Regulatory Secretariat Division (MVCB), 1800 F Street,
Washington, DC 20405, telephone 202-501-4755. Please cite OMB Control
No. 9000-0056, Report of Shipment, in all correspondence.
Dated: June 9, 2016.
Lorin S. Curit,
Director, Federal Acquisition Policy Division, Office of Governmentwide
Acquisition Policy, Office of Acquisition Policy, Office of
Governmentwide Policy.
[FR Doc. 2016-14119 Filed 6-14-16; 8:45 am]
BILLING CODE 6820-EP-P