Agency Forms Undergoing Paperwork Reduction Act Review, 18624-18626 [2015-07839]
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18624
Federal Register / Vol. 80, No. 66 / Tuesday, April 7, 2015 / Notices
b. Interest Rate Spread
FEDERAL RESERVE SYSTEM
Currently, the FR 2420 report does not
have an ‘‘interest rate spread’’ reporting
field. Without this field, the underlying
value of the reference rate and spread
components cannot be determined with
certainty. Accordingly, the Board
proposes to add an ‘‘interest rate
spread’’ field to the FR 2420 report. This
new reporting field will enable
calculation of the value of the
underlying reference rate without
looking up the reference rate in an
additional data source. This field would
be labelled ‘NA’ for fixed-rate CDs.
Formations of, Acquisitions by, and
Mergers of Bank Holding Companies
c. Option Identifiers and Step-Up
Indicator
mstockstill on DSK4VPTVN1PROD with NOTICES
The Board proposes to add report
fields to the FR 2420 that would identify
CDs with embedded options as well as
CDs and time deposits with rates that
change over the term of the CD. CDs
with options are becoming an
increasingly important financial
instrument with growing issuance,
particularly in products with options to
extend the maturity date. One
additional data field would need to be
added to identify instruments with
embedded options. In addition,
experience with the current data
suggests that there is also a segment of
the CD market with rates that rise or
‘‘step up’’ over the course of the
instrument’s life. An additional field
would be necessary to identify these
transactions. These fields could be
particularly important for informing the
use of CD rates in the calculation of
reference rates, as options affect the
comparability of instruments to others
with the same stated maturity dates.
• CDs with embedded options would
be identified under the proposal with an
additional field that would capture the
type of option, specifically ‘callable,’
‘puttable,’ ‘extendable,’ and ‘other,’ or
indicate ‘NA’ for CDs without
embedded options.
• Rates that will rise or fall over the
life of the time deposit or CD based on
a pre-arranged agreement would be
identified under the proposal with an
additional field that would be a ‘Y’ or
‘N’ step-up indicator.
Board of Governors of the Federal Reserve
System, April 2, 2015.
Robert deV. Frierson,
Secretary of the Board.
[FR Doc. 2015–07920 Filed 4–6–15; 8:45 am]
BILLING CODE CODE 6210–01–P
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17:46 Apr 06, 2015
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The companies listed in this notice
have applied to the Board for approval,
pursuant to the Bank Holding Company
Act of 1956 (12 U.S.C. 1841 et seq.)
(BHC Act), Regulation Y (12 CFR part
225), and all other applicable statutes
and regulations to become a bank
holding company and/or to acquire the
assets or the ownership of, control of, or
the power to vote shares of a bank or
bank holding company and all of the
banks and nonbanking companies
owned by the bank holding company,
including the companies listed below.
The applications listed below, as well
as other related filings required by the
Board, are available for immediate
inspection at the Federal Reserve Bank
indicated. The applications will also be
available for inspection at the offices of
the Board of Governors. Interested
persons may express their views in
writing on the standards enumerated in
the BHC Act (12 U.S.C. 1842(c)). If the
proposal also involves the acquisition of
a nonbanking company, the review also
includes whether the acquisition of the
nonbanking company complies with the
standards in section 4 of the BHC Act
(12 U.S.C. 1843). Unless otherwise
noted, nonbanking activities will be
conducted throughout the United States.
Unless otherwise noted, comments
regarding each of these applications
must be received at the Reserve Bank
indicated or the offices of the Board of
Governors not later than May 1, 2015.
A. Federal Reserve Bank of Cleveland
(Nadine Wallman, Vice President) 1455
East Sixth Street, Cleveland, Ohio
44101–2566:
1. Farmers National Banc Corp,
Canfield, Ohio; to acquire 100 percent of
the voting shares of National Bancshares
Corp, Orrville, Ohio and thereby
indirectly acquire First National Bank,
Orrville, Ohio.
B. Federal Reserve Bank of Atlanta
(Chapelle Davis, Assistant Vice
President) 1000 Peachtree Street NE.,
Atlanta, Georgia 30309:
1. American Commerce Bancshares,
Inc., Breman, Georgia; to acquire 100
percent of the voting shares of ProBank,
Tallahassee, Florida.
C. Federal Reserve Bank of
Minneapolis (Jacquelyn K. Brunmeier,
Assistant Vice President) 90 Hennepin
Avenue, Minneapolis, Minnesota
55480–0291:
1. Inter-Mountain Bancorp, Inc.,
Bozeman, Montana; to merge with Teton
Bancshares, Inc., and thereby indirectly
acquire Teton Banks, both in Fairfield,
Montana.
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Fmt 4703
Sfmt 4703
Board of Governors of the Federal Reserve
System, April 2, 2015.
Michael J. Lewandowski,
Associate Secretary of the Board.
[FR Doc. 2015–07901 Filed 4–6–15; 8:45 am]
BILLING CODE CODE 6210–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[30Day–15–0740]
Agency Forms Undergoing Paperwork
Reduction Act Review
The Centers for Disease Control and
Prevention (CDC) has submitted the
following information collection request
to the Office of Management and Budget
(OMB) for review and approval in
accordance with the Paperwork
Reduction Act of 1995. The notice for
the proposed information collection is
published to obtain comments from the
public and affected agencies.
Written comments and suggestions
from the public and affected agencies
concerning the proposed collection of
information are encouraged. Your
comments should address any of the
following: (a) Evaluate whether the
proposed collection of information is
necessary for the proper performance of
the functions of the agency, including
whether the information will have
practical utility; (b) Evaluate the
accuracy of the agencies estimate of the
burden of the proposed collection of
information, including the validity of
the methodology and assumptions used;
(c) Enhance the quality, utility, and
clarity of the information to be
collected; (d) Minimize the burden of
the collection of information on those
who are to respond, including through
the use of appropriate automated,
electronic, mechanical, or other
technological collection techniques or
other forms of information technology,
e.g., permitting electronic submission of
responses; and (e) Assess information
collection costs.
To request additional information on
the proposed project or to obtain a copy
of the information collection plan and
instruments, call (404) 639–7570 or
send an email to omb@cdc.gov. Written
comments and/or suggestions regarding
the items contained in this notice
should be directed to the Attention:
CDC Desk Officer, Office of Management
and Budget, Washington, DC 20503 or
by fax to (202) 395–5806. Written
comments should be received within 30
days of this notice.
E:\FR\FM\07APN1.SGM
07APN1
18625
Federal Register / Vol. 80, No. 66 / Tuesday, April 7, 2015 / Notices
Proposed Project
Medical Monitoring Project (MMP)—
(OMB Control No. 0920–0740
Expiration: 5/31/2015)—Revision—
National Center for HIV/AIDS, Viral
Hepatitis, STD, and TB Prevention
(NCHHSTP), Centers for Disease Control
and Prevention (CDC).
Background and Brief Description
The Centers for Disease Control and
Prevention (CDC), Division of HIV/AIDS
Prevention (DHAP) requests a revision
of the currently approved Information
Collection Request: ‘‘Medical
Monitoring Project’’ expiring May 31,
2015. This data collection addresses the
need for national estimates of access to
and utilization of HIV-related medical
care and services, the quality of HIVrelated ambulatory care, and HIVrelated behaviors and clinical outcomes.
For the proposed project, the same
data collection methods will be used as
for the currently approved project. Data
would be collected from a probability
sample of HIV-diagnosed adults in the
U.S. who consent to an interview and
abstraction of their medical records. As
for the currently approved project, deidentified information would also be
extracted from HIV case surveillance
records for a dataset, referred to as the
minimum dataset, which is used to
assess non-response bias, for quality
control, to improve the ability of MMP
to monitor ongoing care and treatment
of HIV-infected persons, and to make
inferences from the MMP sample to
HIV-diagnosed persons nationally. No
other Federal agency collects such
nationally representative populationbased information from HIV-diagnosed
adults. The data are expected to have
significant implications for policy,
program development, and resource
allocation at the state/local and national
levels.
The changes proposed in this request
update the data collection system to
meet prevailing information needs and
enhance the value of MMP data, while
remaining within the scope of the
currently approved project purpose. The
result is a 16% reduction in burden, or
a reduction of 1,397 total burden hours
annually.
• A change in sampling methods
accounts for the net reduction in
burden. Specifically, sampling from the
existing HIV case surveillance database,
the National HIV Surveillance System
(NHSS, OMB Control No. 0920–0573,
Exp. 2/29/2016) would replace the
current health care-facility-based
sampling. This change in sampling
methods would broaden participation in
MMP to all HIV-infected persons who
have been diagnosed and reported to the
NHSS, a population that is more
representative of persons living with
HIV than are persons receiving HIV
medical care. Sampling from NHSS will
allow MMP to address key information
gaps related to increasing access to care,
one of three strategic areas of national
focus of the National HIV/AIDS
Strategy. The change in project
sampling methods reduces the amount
of time health care facility staff will
spend on project activities, substantially
reducing burden hours and offsetting
increases in burden from other changes,
listed below. Restoration of the original
sample of 26 geographic primary
sampling units is proposed in this
request, for more complete coverage of
the population of interest. Three project
areas that initially participated in
MMP—and were subsequently dropped
in 2009 because funding was
restricted—will be reinstated as primary
sampling units if funding allows.
• Increasing the sample size in three
areas that were previously allocated
comparatively small samples (Georgia,
Illinois, and Pennsylvania) is expected
to improve the ability to produce
representative local estimates in these
areas.
• Health care facility staff may be
asked to look up contact information for
sampled persons with incomplete or
incorrect contact information in NHSS;
this was not necessary in prior MMP
cycles because the patient samples were
drawn from facility records.
Finally, changes were made that did
not affect the burden, listed below:
• The interview instrument was
revised to enable the collection of
critical information from HIV-infected
persons not receiving medical care and
to improve question coherence, boost
the efficiency of the data collection, and
increase the relevance and value of the
information. These changes were based
on an evaluation of the currently
approved MMP interview instrument
involving stakeholders, as well as a pilot
which evaluated new questions
(Formative Research and Tool
Development, OMB Control No. 0920–
0840, expiration 2/29/2016). These
revisions did not change the average
time required to complete the interview.
• Six data elements were removed
from the medical record abstraction
form and two data elements were added.
Because the medical records are
abstracted by MMP staff, these changes
do not affect the burden of the project
on the public.
• Sampled persons may be
interviewed wherever they currently
reside, conditional on local law and
policy, and in a manner specified by a
written, project-specific agreement with
the HIV surveillance unit at the person’s
local health department.
• Videoconferencing was added as an
optional mode of interview
administration. Administering the
interview via videoconferencing will
provide more flexibility for participating
in the interview and facilitate
communication between respondent
and interviewer, for example, by
allowing interviewers to respond
appropriately to a respondent’s visual
cues. Videoconferencing will also allow
the interviewer to ensure that the
respondent is using the correct response
cards for interview questions. No audio/
audiovisual recordings will be made of
the interviews, including interviews
administered by videoconferencing.
This proposed data collection would
supplement the National HIV
Surveillance System (NHSS, OMB
Control No. 0920–0573, Exp. 2/29/2016)
in 26 selected state and local health
departments, which collect information
on persons diagnosed with, living with,
and dying from HIV infection and AIDS.
The participation of respondents is
voluntary. There is no cost to the
respondents other than their time.
Through their participation,
respondents will help to improve
programs to prevent HIV infection as
well as services for those who already
have HIV. The total burden hours are
7,140.
mstockstill on DSK4VPTVN1PROD with NOTICES
ESTIMATED ANNUALIZED BURDEN HOURS
Number of
respondents
Type of respondent
Form name
Sampled, Eligible HIV-Infected Persons ...........................
Facility office staff looking up contact information ............
Interview Questionnaire ...............
N/A ...............................................
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17:46 Apr 06, 2015
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Fmt 4703
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E:\FR\FM\07APN1.SGM
8,720
2,180
07APN1
Number of
responses per
respondent
1
1
Average
hours per
response
(in hours)
45/60
2/60
18626
Federal Register / Vol. 80, No. 66 / Tuesday, April 7, 2015 / Notices
ESTIMATED ANNUALIZED BURDEN HOURS—Continued
Number of
respondents
Number of
responses per
respondent
Average
hours per
response
(in hours)
Type of respondent
Form name
Facility office staff approaching sampled persons for enrollment.
Facility office staff pulling medical records .......................
N/A ...............................................
1,090
1
5/60
N/A ...............................................
8,720
1
3/60
Leroy A. Richardson
Chief, Information Collection Review Office,
Office of Scientific Integrity, Office of the
Associate Director for Science, Office of the
Director, Centers for Disease Control and
Prevention.
[FR Doc. 2015–07839 Filed 4–6–15; 8:45 am]
BILLING CODE CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[30Day–15–15UK]
mstockstill on DSK4VPTVN1PROD with NOTICES
Agency Forms Undergoing Paperwork
Reduction Act Review
The Centers for Disease Control and
Prevention (CDC) has submitted the
following information collection request
to the Office of Management and Budget
(OMB) for review and approval in
accordance with the Paperwork
Reduction Act of 1995. The notice for
the proposed information collection is
published to obtain comments from the
public and affected agencies.
Written comments and suggestions
from the public and affected agencies
concerning the proposed collection of
information are encouraged. Your
comments should address any of the
following: (a) Evaluate whether the
proposed collection of information is
necessary for the proper performance of
the functions of the agency, including
whether the information will have
practical utility; (b) Evaluate the
accuracy of the agencies estimate of the
burden of the proposed collection of
information, including the validity of
the methodology and assumptions used;
(c) Enhance the quality, utility, and
clarity of the information to be
collected; (d) Minimize the burden of
the collection of information on those
who are to respond, including through
the use of appropriate automated,
electronic, mechanical, or other
technological collection techniques or
other forms of information technology,
e.g., permitting electronic submission of
responses; and (e) Assess information
collection costs.
VerDate Sep<11>2014
17:46 Apr 06, 2015
Jkt 235001
To request additional information on
the proposed project or to obtain a copy
of the information collection plan and
instruments, call (404) 639–7570 or
send an email to omb@cdc.gov. Written
comments and/or suggestions regarding
the items contained in this notice
should be directed to the Attention:
CDC Desk Officer, Office of Management
and Budget, Washington, DC 20503 or
by fax to (202) 395–5806. Written
comments should be received within 30
days of this notice.
Proposed Project
Generic Clearance for the Collection
of Qualitative Feedback on Agency
Service Delivery—NEW—National
Center for Emerging and Zoonotic
Infectious Diseases, Centers for Disease
Control and Prevention (CDC).
As part of a Federal Government-wide
effort to streamline the process to seek
feedback from the public on service
delivery, the CDC has submitted a
Generic Information Collection Request
(Generic ICR): ‘‘Generic Clearance for
the Collection of Qualitative Feedback
on Agency Service Delivery’’ to OMB for
approval under the Paperwork
Reduction Act (PRA) (44 U.S.C. 3501 et
seq.).
Background and Brief Description
The information collection activity
will garner qualitative customer and
stakeholder feedback in an efficient,
timely manner, in accordance with the
Administration’s commitment to
improving service delivery. By
qualitative feedback we mean
information that provides useful
insights on perceptions and opinions,
but are not statistical surveys that yield
quantitative results that can be
generalized to the population of study.
This feedback will provide insights into
customer or stakeholder perceptions,
experiences and expectations, provide
an early warning of issues with service,
or focus attention on areas where
communication, training or changes in
operations might improve delivery of
products or services. These collections
will allow for ongoing, collaborative and
actionable communications between the
PO 00000
Frm 00041
Fmt 4703
Sfmt 4703
Agency and its customers and
stakeholders. It will also allow feedback
to contribute directly to the
improvement of program management.
Feedback collected under this generic
clearance will provide useful
information, but it will not yield data
that can be generalized to the overall
population. This type of generic
clearance for qualitative information
will not be used for quantitative
information collections that are
designed to yield reliably actionable
results, such as monitoring trends over
time or documenting program
performance. Such data uses require
more rigorous designs that address: The
target population to which
generalizations will be made, the
sampling frame, the sample design
(including stratification and clustering),
the precision requirements or power
calculations that justify the proposed
sample size, the expected response rate,
methods for assessing potential nonresponse bias, the protocols for data
collection, and any testing procedures
that were or will be undertaken prior to
fielding the study. Depending on the
degree of influence the results are likely
to have, such collections may still be
eligible for submission for other generic
mechanisms that are designed to yield
quantitative results.
In accordance with 5 CFR 1320.8(d),
Vol. 79, No. 83/Wednesday, April 30,
2014, a 60 day notice for public
comment was published in the Federal
Register. No public comments were
received in response to this notice.
This is a new collection of
information. Respondents will take
online surveys or participate in Web site
usability testing, interviews, discussion
groups, or focus groups. Below is
Centers for Disease Control and
Prevention (CDC), National Center for
Emerging and Zoonotic Infectious
Diseases (NCEZID) projected estimate
for the next three years. There is no cost
to respondents other than their time.
The estimated annualized burden hours
for this data collection activity is 3,850
hours:
E:\FR\FM\07APN1.SGM
07APN1
]]>Agencies
[Federal Register Volume 80, Number 66 (Tuesday, April 7, 2015)]
[Notices]
[Pages 18624-18626]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2015-07839]
=======================================================================
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[30Day-15-0740]
Agency Forms Undergoing Paperwork Reduction Act Review
The Centers for Disease Control and Prevention (CDC) has submitted
the following information collection request to the Office of
Management and Budget (OMB) for review and approval in accordance with
the Paperwork Reduction Act of 1995. The notice for the proposed
information collection is published to obtain comments from the public
and affected agencies.
Written comments and suggestions from the public and affected
agencies concerning the proposed collection of information are
encouraged. Your comments should address any of the following: (a)
Evaluate whether the proposed collection of information is necessary
for the proper performance of the functions of the agency, including
whether the information will have practical utility; (b) Evaluate the
accuracy of the agencies estimate of the burden of the proposed
collection of information, including the validity of the methodology
and assumptions used; (c) Enhance the quality, utility, and clarity of
the information to be collected; (d) Minimize the burden of the
collection of information on those who are to respond, including
through the use of appropriate automated, electronic, mechanical, or
other technological collection techniques or other forms of information
technology, e.g., permitting electronic submission of responses; and
(e) Assess information collection costs.
To request additional information on the proposed project or to
obtain a copy of the information collection plan and instruments, call
(404) 639-7570 or send an email to omb@cdc.gov. Written comments and/or
suggestions regarding the items contained in this notice should be
directed to the Attention: CDC Desk Officer, Office of Management and
Budget, Washington, DC 20503 or by fax to (202) 395-5806. Written
comments should be received within 30 days of this notice.
[[Page 18625]]
Proposed Project
Medical Monitoring Project (MMP)--(OMB Control No. 0920-0740
Expiration: 5/31/2015)--Revision--National Center for HIV/AIDS, Viral
Hepatitis, STD, and TB Prevention (NCHHSTP), Centers for Disease
Control and Prevention (CDC).
Background and Brief Description
The Centers for Disease Control and Prevention (CDC), Division of
HIV/AIDS Prevention (DHAP) requests a revision of the currently
approved Information Collection Request: ``Medical Monitoring Project''
expiring May 31, 2015. This data collection addresses the need for
national estimates of access to and utilization of HIV-related medical
care and services, the quality of HIV-related ambulatory care, and HIV-
related behaviors and clinical outcomes.
For the proposed project, the same data collection methods will be
used as for the currently approved project. Data would be collected
from a probability sample of HIV-diagnosed adults in the U.S. who
consent to an interview and abstraction of their medical records. As
for the currently approved project, de-identified information would
also be extracted from HIV case surveillance records for a dataset,
referred to as the minimum dataset, which is used to assess non-
response bias, for quality control, to improve the ability of MMP to
monitor ongoing care and treatment of HIV-infected persons, and to make
inferences from the MMP sample to HIV-diagnosed persons nationally. No
other Federal agency collects such nationally representative
population-based information from HIV-diagnosed adults. The data are
expected to have significant implications for policy, program
development, and resource allocation at the state/local and national
levels.
The changes proposed in this request update the data collection
system to meet prevailing information needs and enhance the value of
MMP data, while remaining within the scope of the currently approved
project purpose. The result is a 16% reduction in burden, or a
reduction of 1,397 total burden hours annually.
A change in sampling methods accounts for the net
reduction in burden. Specifically, sampling from the existing HIV case
surveillance database, the National HIV Surveillance System (NHSS, OMB
Control No. 0920-0573, Exp. 2/29/2016) would replace the current health
care-facility-based sampling. This change in sampling methods would
broaden participation in MMP to all HIV-infected persons who have been
diagnosed and reported to the NHSS, a population that is more
representative of persons living with HIV than are persons receiving
HIV medical care. Sampling from NHSS will allow MMP to address key
information gaps related to increasing access to care, one of three
strategic areas of national focus of the National HIV/AIDS Strategy.
The change in project sampling methods reduces the amount of time
health care facility staff will spend on project activities,
substantially reducing burden hours and offsetting increases in burden
from other changes, listed below. Restoration of the original sample of
26 geographic primary sampling units is proposed in this request, for
more complete coverage of the population of interest. Three project
areas that initially participated in MMP--and were subsequently dropped
in 2009 because funding was restricted--will be reinstated as primary
sampling units if funding allows.
Increasing the sample size in three areas that were
previously allocated comparatively small samples (Georgia, Illinois,
and Pennsylvania) is expected to improve the ability to produce
representative local estimates in these areas.
Health care facility staff may be asked to look up contact
information for sampled persons with incomplete or incorrect contact
information in NHSS; this was not necessary in prior MMP cycles because
the patient samples were drawn from facility records.
Finally, changes were made that did not affect the burden, listed
below:
The interview instrument was revised to enable the
collection of critical information from HIV-infected persons not
receiving medical care and to improve question coherence, boost the
efficiency of the data collection, and increase the relevance and value
of the information. These changes were based on an evaluation of the
currently approved MMP interview instrument involving stakeholders, as
well as a pilot which evaluated new questions (Formative Research and
Tool Development, OMB Control No. 0920-0840, expiration 2/29/2016).
These revisions did not change the average time required to complete
the interview.
Six data elements were removed from the medical record
abstraction form and two data elements were added. Because the medical
records are abstracted by MMP staff, these changes do not affect the
burden of the project on the public.
Sampled persons may be interviewed wherever they currently
reside, conditional on local law and policy, and in a manner specified
by a written, project-specific agreement with the HIV surveillance unit
at the person's local health department.
Videoconferencing was added as an optional mode of
interview administration. Administering the interview via
videoconferencing will provide more flexibility for participating in
the interview and facilitate communication between respondent and
interviewer, for example, by allowing interviewers to respond
appropriately to a respondent's visual cues. Videoconferencing will
also allow the interviewer to ensure that the respondent is using the
correct response cards for interview questions. No audio/audiovisual
recordings will be made of the interviews, including interviews
administered by videoconferencing.
This proposed data collection would supplement the National HIV
Surveillance System (NHSS, OMB Control No. 0920-0573, Exp. 2/29/2016)
in 26 selected state and local health departments, which collect
information on persons diagnosed with, living with, and dying from HIV
infection and AIDS.
The participation of respondents is voluntary. There is no cost to
the respondents other than their time. Through their participation,
respondents will help to improve programs to prevent HIV infection as
well as services for those who already have HIV. The total burden hours
are 7,140.
Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Number of Average hours
Type of respondent Form name Number of responses per per response
respondents respondent (in hours)
----------------------------------------------------------------------------------------------------------------
Sampled, Eligible HIV-Infected Persons Interview Questionnaire. 8,720 1 45/60
Facility office staff looking up N/A..................... 2,180 1 2/60
contact information.
[[Page 18626]]
Facility office staff approaching N/A..................... 1,090 1 5/60
sampled persons for enrollment.
Facility office staff pulling medical N/A..................... 8,720 1 3/60
records.
----------------------------------------------------------------------------------------------------------------
Leroy A. Richardson
Chief, Information Collection Review Office, Office of Scientific
Integrity, Office of the Associate Director for Science, Office of the
Director, Centers for Disease Control and Prevention.
[FR Doc. 2015-07839 Filed 4-6-15; 8:45 am]
BILLING CODE CODE 4163-18-P
