Agency Information Collection Activities: Proposed Collection; Comment Request; Current Good Manufacturing Practice Regulations for Medicated Feeds, 19091-19093 [2014-07646]
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<![CDATA[
19091
Federal Register / Vol. 79, No. 66 / Monday, April 7, 2014 / Notices
ANNUAL BURDEN ESTIMATES
Annual
number of
respondents
Instrument
RISE
RISE
RISE
RISE
RISE
RISE
RISE
RISE
CCT
CCT
CCT
CCT
CCT
CCT
CCT
CCT
Number of
responses per
respondent
Average
burden hours
per response
Total annual
burden hours
Youth Interview (ages 11–19) .......................................................
Qualitative Youth Interview (ages 11–19) .....................................
Facilitator Interview (Facilitator Burden) ........................................
Facilitator Interview (Child burden) ................................................
Facilitator Survey ...........................................................................
Facilitator submission of CAFAS data 1 ........................................
Permanency Resource Interview ...................................................
Interview with Current Caregiver ...................................................
22
22
2
3
2
2
11
11
2
1
4
2
21
21
2
2
1.3
1.2
0.2
.5
0.2
0.1
1.0
0.6
57
26
2
3
8
4
22
13
RISE CCT burden ....................................................................................
........................
........................
........................
135
RISE ORB Staff Follow-Up Survey .................................................................
157
1
0.3
47
RISE ORB burden ....................................................................................
........................
........................
........................
47
Cost Study Focus Group Preparation .............................................................
Cost Study Focus Group .................................................................................
Trial Administration of Cost Study Activity Logs .............................................
Weekly Case Work Activity Log ......................................................................
Weekly Supervision Activity Log ......................................................................
Monthly Management/Administration Log .......................................................
9
9
9
123
39
30
1
1
1
52
52
12
1.5
4.0
1.5
0.4
0.4
0.5
14
36
14
2,558
811
180
Cost study burden ....................................................................................
........................
........................
........................
3,613
Administrative data submission, no added fields ............................................
Administrative data submission with added fields ...........................................
1
1
12
12
0.3
0.8
2
10
Administrative data study burden .............................................................
........................
........................
........................
12
mstockstill on DSK4VPTVN1PROD with NOTICES
1 The
CAFAS is administered as part of case planning, so the only burden is in submitting the CAFAS data to the evaluation team.
Estimated Total Annual Burden
Hours: 3,807.
Additional Information: Copies of the
proposed collection may be obtained by
writing to the Administration for
Children and Families, Office of
Planning, Research and Evaluation, 370
L’Enfant Promenade SW., Washington,
DC 20447, Attn: OPRE Reports
Clearance Officer. All requests should
be identified by the title of the
information collection. Email address:
OPREinfocollection@acf.hhs.gov.
OMB Comment: OMB is required to
make a decision concerning the
collection of information between 30
and 60 days after publication of this
document in the Federal Register.
Therefore, a comment is best assured of
having its full effect if OMB receives it
within 30 days of publication. Written
comments and recommendations for the
proposed information collection should
be sent directly to the following: Office
of Management and Budget, Paperwork
Reduction Project, Email: OIRA_
SUBMISSION@OMB.EOP.GOV, Attn:
Desk Officer for the Administration for
Children and Families.
Karl Koerper,
OPRE Reports Clearance Officer.
[FR Doc. 2014–07614 Filed 4–4–14; 8:45 am]
BILLING CODE 4184–01–P
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17:49 Apr 04, 2014
Jkt 232001
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2004–N–0193]
Agency Information Collection
Activities: Proposed Collection;
Comment Request; Current Good
Manufacturing Practice Regulations for
Medicated Feeds
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Notice.
The Food and Drug
Administration (FDA) is announcing an
opportunity for public comment on the
proposed collection of certain
information by the Agency. Under the
Paperwork Reduction Act of 1995 (the
PRA), Federal Agencies are required to
publish notice in the Federal Register
concerning each proposed collection of
information, including each proposed
extension of an existing collection of
information, and to allow 60 days for
public comment in response to the
notice. This notice solicits comments on
the recordkeeping requirements for
manufacturers of medicated animal
feeds.
SUMMARY:
PO 00000
Frm 00047
Fmt 4703
Sfmt 4703
Submit either electronic or
written comments on the collection of
information by June 6, 2014.
ADDRESSES: Submit electronic
comments on the collection of
information to https://
www.regulations.gov. Submit written
comments on the collection of
information to the Division of Dockets
Management (HFA–305), Food and Drug
Administration, 5630 Fishers Lane, Rm.
1061, Rockville, MD 20852. All
comments should be identified with the
docket number found in brackets in the
heading of this document.
FOR FURTHER INFORMATION CONTACT: FDA
PRA Staff, Office of Operations, Food
and Drug Administration, 1350 Piccard
Dr., PI50–400B, Rockville, MD 20850,
PRAStaff@fda.hhs.gov.
SUPPLEMENTARY INFORMATION: Under the
PRA (44 U.S.C. 3501–3520), Federal
Agencies must obtain approval from the
Office of Management and Budget
(OMB) for each collection of
information they conduct or sponsor.
‘‘Collection of information’’ is defined
in 44 U.S.C. 3502(3) and 5 CFR
1320.3(c) and includes Agency requests
or requirements that members of the
public submit reports, keep records, or
provide information to a third party.
Section 3506(c)(2)(A) of the PRA (44
U.S.C. 3506(c)(2)(A)) requires Federal
DATES:
E:\FR\FM\07APN1.SGM
07APN1
19092
Federal Register / Vol. 79, No. 66 / Monday, April 7, 2014 / Notices
Agencies to provide a 60-day notice in
the Federal Register concerning each
proposed collection of information,
including each proposed extension of an
existing collection of information,
before submitting the collection to OMB
for approval. To comply with this
requirement, FDA is publishing notice
of the proposed collection of
information set forth in this document.
With respect to the following
collection of information, FDA invites
comments on these topics: (1) Whether
the proposed collection of information
is necessary for the proper performance
of FDA’s functions, including whether
the information will have practical
utility; (2) the accuracy of FDA’s
estimate of the burden of the proposed
collection of information, including the
validity of the methodology and
assumptions used; (3) ways to enhance
the quality, utility, and clarity of the
information to be collected; and (4)
ways to minimize the burden of the
collection of information on
respondents, including through the use
of automated collection techniques,
when appropriate, and other forms of
information technology.
Current Good Manufacturing Practice
Regulations for Medicated Feeds—21
CFR Part 225 (OMB Control Number
0910–0152)—Extension
Under section 501 of the Federal
Food, Drug, and Cosmetic Act (the
FD&C Act) (21 U.S.C. 351), FDA has the
statutory authority to issue current good
manufacturing practice (cGMP)
regulations for drugs, including
medicated feeds. Medicated feeds are
administered to animals for the
prevention, cure, mitigation, or
treatment of disease, or growth
promotion and feed efficiency. Statutory
requirements for cGMPs have been
codified under part 225 (21 CFR part
225). Medicated feeds that are not
manufactured in accordance with these
regulations are considered adulterated
under section 501(a)(2)(B) of the FD&C
Act. Under part 225, a manufacturer is
required to establish, maintain, and
retain records for a medicated feed,
including records to document
procedures required during the
manufacturing process to assure that
proper quality control is maintained.
Such records would, for example,
contain information concerning receipt
and inventory of drug components,
batch production, laboratory assay
results (i.e. batch and stability testing),
labels, and product distribution.
This information is needed so that
FDA can monitor drug usage and
possible misformulation of medicated
feeds to investigate violative drug
residues in products from treated
animals and to investigate product
defects when a drug is recalled. In
addition, FDA will use the cGMP
criteria in part 225 to determine
whether or not the systems and
procedures used by manufacturers of
medicated feeds are adequate to assure
that their feeds meet the requirements of
the act as to safety and also that they
meet their claimed identity, strength,
quality, and purity, as required by
section 501(a)(2)(B) of the FD&C Act.
A license is required when the
manufacturer of a medicated feed
involves the use of a drug or drugs that
FDA has determined requires more
control because of the need for a
withdrawal period before slaughter or
because of carcinogenic concerns.
Conversely, a license is not required and
the recordkeeping requirements are less
demanding for those medicated feeds
for which FDA has determined that the
drugs used in their manufacture need
less control. Respondents to this
collection of information are
commercial feed mills and mixerfeeders.
FDA estimates the burden of this
collection of information as follows:
TABLE 1—ESTIMATED ANNUAL RECORDKEEPING BURDEN
[Registered licensed commercial feed mills] 1
Number of
recordkeepers
21 CFR Section
Number of
records per
recordkeeper
225.42(b)(5) through (b)(8) .............................................
225.58(c) and (d) ............................................................
225.80(b)(2) .....................................................................
225.102(b)(1) ...................................................................
225.110(b)(1) and (b)(2) .................................................
225.115(b)(1) and (b)(2) .................................................
840
840
840
840
840
840
260
45
1,600
7,800
7,800
5
218,400
37,800
1,344,000
6,552,000
6,552,000
4,200
Total .........................................................................
........................
........................
........................
1 There
Average
burden per
recordkeeper
Total annual
records
1
.50 (30 minutes)
.12 (7 minutes)
.08 (5 minutes)
.015 (1 minute)
.12 (7 minutes)
............................
Total hours
218,400
18,900
161,280
524,160
98,280
504
1,021,524
are no capital or operating and maintenance costs associated with this collection of information.
TABLE 2—ESTIMATED ANNUAL RECORDKEEPING BURDEN
[Registered licensed mixer-feeders] 1
Number of
recordkeepers
mstockstill on DSK4VPTVN1PROD with NOTICES
21 CFR Section
Number of
records per
recordkeeper
225.42(b)(5) through (b)(8) .............................................
225.58(c) and (d) ............................................................
225.80(b)(2) .....................................................................
225.102(b)(1) through (b)(5) ...........................................
100
100
100
100
260
36
48
260
26,000
3,600
4,800
26,000
Total .........................................................................
........................
........................
........................
1 There
Average
burden per
recordkeeper
Total annual
records
.15
.50
.12
.40
(9 minutes)
(30 minutes)
(7 minutes)
(24 minutes)
3,900
1,800
576
10,400
............................
16,676
are no capital costs or operating and maintenance costs associated with this collection of information.
VerDate Mar<15>2010
17:49 Apr 04, 2014
Jkt 232001
PO 00000
Frm 00048
Fmt 4703
Sfmt 4703
E:\FR\FM\07APN1.SGM
Total hours
07APN1
Federal Register / Vol. 79, No. 66 / Monday, April 7, 2014 / Notices
19093
TABLE 3—ESTIMATED ANNUAL RECORDKEEPING BURDEN
[Nonregistered unlicensed commercial feed mills] 1
Number of
recordkeepers
21 CFR Section
225.142
225.158
225.180
225.202
Number of
records per
recordkeeper
...........................................................................
...........................................................................
...........................................................................
...........................................................................
4,186
4,186
4,186
4,186
4
1
96
260
16,744
4,186
401,856
1,088,360
Total .........................................................................
........................
........................
........................
1 There
Average
burden per
recordkeeper
Total annual
records
Total hours
1
4
.12 (7 minutes)
.65 (39 minutes)
16,744
16,744
48,223
707,434
............................
789,145
are no capital costs or operating and maintenance costs associated with this collection of information.
TABLE 4—ESTIMATED ANNUAL RECORDKEEPING BURDEN
[Nonregistered unlicensed mixer-feeders] 1
Number of
recordkeepers
21 CFR Section
225.142
225.158
225.180
225.202
Number of
records per
recordkeeper
...........................................................................
...........................................................................
...........................................................................
...........................................................................
3,400
3,400
3,400
3,400
4
1
32
260
13,600
3,400
108,800
884,000
Total .........................................................................
........................
........................
........................
1 There
Dated: March 28, 2014.
Leslie Kux,
Assistant Commissioner for Policy.
[FR Doc. 2014–07646 Filed 4–4–14; 8:45 am]
BILLING CODE 4164–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2004–N–0389]
Agency Information Collection
Activities; Proposed Collection;
Comment Request; Current Good
Manufacturing Practice Regulations for
Type A Medicated Articles
Food and Drug Administration,
mstockstill on DSK4VPTVN1PROD with NOTICES
HHS.
ACTION:
Total hours
1
4
.12 (7 minutes)
.33 (20 minutes)
13,600
13,600
13,056
291,720
............................
331,976
are no capital costs or operating and maintenance costs associated with this collection of information.
The estimate of time required for
record preparation and maintenance is
based on Agency communications with
industry. Other information needed to
finally calculate the total burden hours
(i.e., number of recordkeepers, number
of medicated feeds being manufactured,
etc.) is derived from Agency records and
experience.
AGENCY:
Average
burden per
recordkeeper
Total annual
records
Notice.
The Food and Drug
Administration (FDA) is announcing an
opportunity for public comment on the
proposed collection of certain
information by the Agency. Under the
Paperwork Reduction Act of 1995 (the
PRA), Federal Agencies are required to
SUMMARY:
VerDate Mar<15>2010
18:42 Apr 04, 2014
Jkt 232001
publish notice in the Federal Register
concerning each proposed collection of
information, including each proposed
extension of an existing collection of
information, and allow 60 days for
public comment in response to the
notice. This notice solicits comments on
the recordkeeping requirements for
manufacturers of Type A medicated
articles.
DATES: Submit either electronic or
written comments on the collection of
information by June 6, 2014.
ADDRESSES: Submit electronic
comments on the collection of
information to https://
www.regulations.gov. Submit written
comments on the collection of
information to the Division of Dockets
Management (HFA–305), Food and Drug
Administration, 5630 Fishers Lane, rm.
1061, Rockville, MD 20852. All
comments should be identified with the
docket number found in brackets in the
heading of this document.
FOR FURTHER INFORMATION CONTACT: FDA
PRA Staff, Office of Operations, Food
and Drug Administration, 1350 Piccard
Dr., PI50–400B, Rockville, MD 20850,
PRAStaff@fda.hhs.gov.
SUPPLEMENTARY INFORMATION: Under the
PRA, 44 U.S.C. 3501–3520, Federal
Agencies must obtain approval from the
Office of Management and Budget
(OMB) for each collection of
information they conduct or sponsor.
‘‘Collection of information’’ is defined
in 44 U.S.C. 3502(3) and 5 CFR
PO 00000
Frm 00049
Fmt 4703
Sfmt 4703
1320.3(c) and includes Agency requests
or requirements that members of the
public submit reports, keep records, or
provide information to a third party.
Section 3506(c)(2)(A) of the PRA (44
U.S.C. 3506(c)(2)(A)) requires Federal
Agencies to provide a 60-day notice in
the Federal Register concerning each
proposed collection of information,
including each proposed reinstatement
of an existing collection of information,
before submitting the collection to OMB
for approval. To comply with this
requirement, FDA is publishing notice
of the proposed collection of
information set forth in this document.
With respect to the following
collection of information, FDA invites
comments on these topics: (1) Whether
the proposed collection of information
is necessary for the proper performance
of FDA’s functions, including whether
the information will have practical
utility; (2) the accuracy of FDA’s
estimate of the burden of the proposed
collection of information, including the
validity of the methodology and
assumptions used; (3) ways to enhance
the quality, utility, and clarity of the
information to be collected; and (4)
ways to minimize the burden of the
collection of information on
respondents, including through the use
of automated collection techniques,
when appropriate, and other forms of
information technology.
E:\FR\FM\07APN1.SGM
07APN1
]]>Agencies
[Federal Register Volume 79, Number 66 (Monday, April 7, 2014)]
[Notices]
[Pages 19091-19093]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2014-07646]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA-2004-N-0193]
Agency Information Collection Activities: Proposed Collection;
Comment Request; Current Good Manufacturing Practice Regulations for
Medicated Feeds
AGENCY: Food and Drug Administration, HHS.
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: The Food and Drug Administration (FDA) is announcing an
opportunity for public comment on the proposed collection of certain
information by the Agency. Under the Paperwork Reduction Act of 1995
(the PRA), Federal Agencies are required to publish notice in the
Federal Register concerning each proposed collection of information,
including each proposed extension of an existing collection of
information, and to allow 60 days for public comment in response to the
notice. This notice solicits comments on the recordkeeping requirements
for manufacturers of medicated animal feeds.
DATES: Submit either electronic or written comments on the collection
of information by June 6, 2014.
ADDRESSES: Submit electronic comments on the collection of information
to https://www.regulations.gov. Submit written comments on the
collection of information to the Division of Dockets Management (HFA-
305), Food and Drug Administration, 5630 Fishers Lane, Rm. 1061,
Rockville, MD 20852. All comments should be identified with the docket
number found in brackets in the heading of this document.
FOR FURTHER INFORMATION CONTACT: FDA PRA Staff, Office of Operations,
Food and Drug Administration, 1350 Piccard Dr., PI50-400B, Rockville,
MD 20850, PRAStaff@fda.hhs.gov.
SUPPLEMENTARY INFORMATION: Under the PRA (44 U.S.C. 3501-3520), Federal
Agencies must obtain approval from the Office of Management and Budget
(OMB) for each collection of information they conduct or sponsor.
``Collection of information'' is defined in 44 U.S.C. 3502(3) and 5 CFR
1320.3(c) and includes Agency requests or requirements that members of
the public submit reports, keep records, or provide information to a
third party. Section 3506(c)(2)(A) of the PRA (44 U.S.C. 3506(c)(2)(A))
requires Federal
[[Page 19092]]
Agencies to provide a 60-day notice in the Federal Register concerning
each proposed collection of information, including each proposed
extension of an existing collection of information, before submitting
the collection to OMB for approval. To comply with this requirement,
FDA is publishing notice of the proposed collection of information set
forth in this document.
With respect to the following collection of information, FDA
invites comments on these topics: (1) Whether the proposed collection
of information is necessary for the proper performance of FDA's
functions, including whether the information will have practical
utility; (2) the accuracy of FDA's estimate of the burden of the
proposed collection of information, including the validity of the
methodology and assumptions used; (3) ways to enhance the quality,
utility, and clarity of the information to be collected; and (4) ways
to minimize the burden of the collection of information on respondents,
including through the use of automated collection techniques, when
appropriate, and other forms of information technology.
Current Good Manufacturing Practice Regulations for Medicated Feeds--21
CFR Part 225 (OMB Control Number 0910-0152)--Extension
Under section 501 of the Federal Food, Drug, and Cosmetic Act (the
FD&C Act) (21 U.S.C. 351), FDA has the statutory authority to issue
current good manufacturing practice (cGMP) regulations for drugs,
including medicated feeds. Medicated feeds are administered to animals
for the prevention, cure, mitigation, or treatment of disease, or
growth promotion and feed efficiency. Statutory requirements for cGMPs
have been codified under part 225 (21 CFR part 225). Medicated feeds
that are not manufactured in accordance with these regulations are
considered adulterated under section 501(a)(2)(B) of the FD&C Act.
Under part 225, a manufacturer is required to establish, maintain, and
retain records for a medicated feed, including records to document
procedures required during the manufacturing process to assure that
proper quality control is maintained. Such records would, for example,
contain information concerning receipt and inventory of drug
components, batch production, laboratory assay results (i.e. batch and
stability testing), labels, and product distribution.
This information is needed so that FDA can monitor drug usage and
possible misformulation of medicated feeds to investigate violative
drug residues in products from treated animals and to investigate
product defects when a drug is recalled. In addition, FDA will use the
cGMP criteria in part 225 to determine whether or not the systems and
procedures used by manufacturers of medicated feeds are adequate to
assure that their feeds meet the requirements of the act as to safety
and also that they meet their claimed identity, strength, quality, and
purity, as required by section 501(a)(2)(B) of the FD&C Act.
A license is required when the manufacturer of a medicated feed
involves the use of a drug or drugs that FDA has determined requires
more control because of the need for a withdrawal period before
slaughter or because of carcinogenic concerns. Conversely, a license is
not required and the recordkeeping requirements are less demanding for
those medicated feeds for which FDA has determined that the drugs used
in their manufacture need less control. Respondents to this collection
of information are commercial feed mills and mixer-feeders.
FDA estimates the burden of this collection of information as
follows:
Table 1--Estimated Annual Recordkeeping Burden
[Registered licensed commercial feed mills] \1\
--------------------------------------------------------------------------------------------------------------------------------------------------------
Number of
21 CFR Section Number of records per Total annual Average burden per recordkeeper Total hours
recordkeepers recordkeeper records
--------------------------------------------------------------------------------------------------------------------------------------------------------
225.42(b)(5) through (b)(8).................... 840 260 218,400 1 218,400
225.58(c) and (d).............................. 840 45 37,800 .50 (30 minutes) 18,900
225.80(b)(2)................................... 840 1,600 1,344,000 .12 (7 minutes) 161,280
225.102(b)(1).................................. 840 7,800 6,552,000 .08 (5 minutes) 524,160
225.110(b)(1) and (b)(2)....................... 840 7,800 6,552,000 .015 (1 minute) 98,280
225.115(b)(1) and (b)(2)....................... 840 5 4,200 .12 (7 minutes) 504
--------------------------------------------------------------------------------------------------------
Total...................................... .............. .............. .............. ....................................... 1,021,524
--------------------------------------------------------------------------------------------------------------------------------------------------------
\1\ There are no capital or operating and maintenance costs associated with this collection of information.
Table 2--Estimated Annual Recordkeeping Burden
[Registered licensed mixer-feeders] \1\
--------------------------------------------------------------------------------------------------------------------------------------------------------
Number of
21 CFR Section Number of records per Total annual Average burden per recordkeeper Total hours
recordkeepers recordkeeper records
--------------------------------------------------------------------------------------------------------------------------------------------------------
225.42(b)(5) through (b)(8).................... 100 260 26,000 .15 (9 minutes) 3,900
225.58(c) and (d).............................. 100 36 3,600 .50 (30 minutes) 1,800
225.80(b)(2)................................... 100 48 4,800 .12 (7 minutes) 576
225.102(b)(1) through (b)(5)................... 100 260 26,000 .40 (24 minutes) 10,400
--------------------------------------------------------------------------------------------------------
Total...................................... .............. .............. .............. ....................................... 16,676
--------------------------------------------------------------------------------------------------------------------------------------------------------
\1\ There are no capital costs or operating and maintenance costs associated with this collection of information.
[[Page 19093]]
Table 3--Estimated Annual Recordkeeping Burden
[Nonregistered unlicensed commercial feed mills] \1\
--------------------------------------------------------------------------------------------------------------------------------------------------------
Number of
21 CFR Section Number of records per Total annual Average burden per recordkeeper Total hours
recordkeepers recordkeeper records
--------------------------------------------------------------------------------------------------------------------------------------------------------
225.142........................................ 4,186 4 16,744 1 16,744
225.158........................................ 4,186 1 4,186 4 16,744
225.180........................................ 4,186 96 401,856 .12 (7 minutes) 48,223
225.202........................................ 4,186 260 1,088,360 .65 (39 minutes) 707,434
--------------------------------------------------------------------------------------------------------
Total...................................... .............. .............. .............. ....................................... 789,145
--------------------------------------------------------------------------------------------------------------------------------------------------------
\1\ There are no capital costs or operating and maintenance costs associated with this collection of information.
Table 4--Estimated Annual Recordkeeping Burden
[Nonregistered unlicensed mixer-feeders] \1\
--------------------------------------------------------------------------------------------------------------------------------------------------------
Number of
21 CFR Section Number of records per Total annual Average burden per recordkeeper Total hours
recordkeepers recordkeeper records
--------------------------------------------------------------------------------------------------------------------------------------------------------
225.142........................................ 3,400 4 13,600 1 13,600
225.158........................................ 3,400 1 3,400 4 13,600
225.180........................................ 3,400 32 108,800 .12 (7 minutes) 13,056
225.202........................................ 3,400 260 884,000 .33 (20 minutes) 291,720
--------------------------------------------------------------------------------------------------------
Total...................................... .............. .............. .............. ....................................... 331,976
--------------------------------------------------------------------------------------------------------------------------------------------------------
\1\ There are no capital costs or operating and maintenance costs associated with this collection of information.
The estimate of time required for record preparation and
maintenance is based on Agency communications with industry. Other
information needed to finally calculate the total burden hours (i.e.,
number of recordkeepers, number of medicated feeds being manufactured,
etc.) is derived from Agency records and experience.
Dated: March 28, 2014.
Leslie Kux,
Assistant Commissioner for Policy.
[FR Doc. 2014-07646 Filed 4-4-14; 8:45 am]
BILLING CODE 4164-01-P
