Kelvin Soto: Debarment Order, 62634-62635 [2014-24814]
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62634
Federal Register / Vol. 79, No. 202 / Monday, October 20, 2014 / Notices
TABLE 3—ESTIMATED ANNUAL THIRD-PARTY DISCLOSURE BURDEN 1—Continued
No. of
respondents
21 CFR section
No. of
responses per
respondent
Total annual
responses
Average
burden per
response
Total hours
610.40(c)(1)(ii) ..........................................................
610.40(h)(2)(ii)(C) and (h)(2)(ii)(D) ..........................
610.40(h)(2)(vi) ........................................................
610.42(a) ..................................................................
610.46(a)(1)(ii)(B) .....................................................
610.46(a)(3) .............................................................
610.46(b)(3) .............................................................
610.47(a)(1)(ii)(B) .....................................................
610.47(a)(3) .............................................................
610.47(b)(3) .............................................................
630.6(a) 3 ..................................................................
630.6(a) 4 ..................................................................
630.6(d)(1) ...............................................................
2,361
40
2,361
1
1,945
1,945
4,961
1,945
1,945
4,961
648
84
63
1.52
12
7.62
1
5.40
5.40
0.35
12.03
12.03
0.41
668.72
53.57
35.71
3,600
480
18,000
1
10,500
10,500
1,755
23,400
23,400
2,050
433,333
4,500
2,250
0.08 (5 minutes) ........
0.20 (12 minutes) ......
0.08 (5 minutes) ........
1 ................................
0.17 (10 minutes) ......
0.17 (10 minutes) ......
1 ................................
0.17 (10 minutes) ......
0.17 (10 minutes) ......
1 ................................
0.08 (5 minutes) ........
1.5 (90 minutes) ........
1 ................................
288
96
1,440
1
1,785
1,785
1,755
3,978
3,978
2,050
34,667
6,750
2,250
Total ..................................................................
........................
........................
........................
....................................
63,019
1 There
are no capital costs or operating and maintenance costs associated with this collection of information.
percent of establishments that fall under CLIA that transfuse blood and components and FDA-registered blood establishments (0.05 ×
4,961 + 2,361 = 366).
3 Notification of donors determined not to be eligible for donation based on failure to satisfy eligibility criteria.
4 Notification of donors deferred based on reactive test results for evidence of infection due to communicable disease agents.
2 Five
Dated: October 14, 2014.
Leslie Kux,
Assistant Commissioner for Policy.
[FR Doc. 2014–24797 Filed 10–17–14; 8:45 am]
BILLING CODE 4164–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2013–N–0960]
Kelvin Soto: Debarment Order
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
SUPPLEMENTARY INFORMATION:
Notice.
I. Background
The Food and Drug
Administration (FDA) is issuing an
order under the Federal Food, Drug, and
Cosmetic Act (the FD&C Act) debarring
Kelvin Soto from providing services in
any capacity to a person that has an
approved or pending drug product
application for a period of 6 years. We
base this order on a finding that Mr.
Soto was convicted of four felony
counts under Federal law for conduct
involving health care fraud and
conspiracy to commit health care fraud
and that this pattern of conduct is
sufficient to find that there is reason to
believe he may violate requirements
under the FD&C Act relating to drug
products. Mr. Soto was given notice of
the proposed debarment and an
opportunity to request a hearing within
the timeframe prescribed by regulation.
Mr. Soto failed to request a hearing. Mr.
Soto’s failure to request a hearing
SUMMARY:
tkelley on DSK3SPTVN1PROD with NOTICES
constitutes a waiver of his right to a
hearing concerning this action.
DATES: This order is effective October
20, 2014.
ADDRESSES: Submit applications for
termination of debarment to the
Division of Dockets Management (HFA–
305), Food and Drug Administration,
5630 Fishers Lane, Rm. 1061, Rockville,
MD 20852.
FOR FURTHER INFORMATION CONTACT:
Kenny Shade, Office of Regulatory
Affairs, Food and Drug Administration,
12420 Parklawn Dr., Element Bldg., Rm.
4144, Rockville, MD 20857, 301–796–
4640.
VerDate Sep<11>2014
17:58 Oct 17, 2014
Jkt 235001
Section 306(b)(2)(B)(ii)(I) of the FD&C
Act (21 U.S.C. 335a(b)(2)(B)(ii)(I))
permits debarment of an individual if
FDA finds that the individual has been
convicted of a felony under Federal law
for conduct that involves bribery;
payment of illegal gratuities; fraud;
perjury; false statement; racketeering;
blackmail; extortion; falsification or
destruction of records; interference
with, obstruction of an investigation
into, or prosecution of any criminal
offense; and FDA finds, on the basis of
the conviction and other information,
that such individual has demonstrated a
pattern of conduct sufficient to find that
there is reason to believe the individual
may violate requirements under the
FD&C Act relating to drug products.
On November 6, 2012, the U.S.
District Court for the Southern District
of Florida entered judgment against Mr.
Soto after a jury found him guilty of four
PO 00000
Frm 00042
Fmt 4703
Sfmt 4703
counts of health care fraud in violation
of 18 U.S.C. 1347 and one count of
conspiracy to commit health care fraud
in violation of 18 U.S.C. 1349.
FDA’s finding that debarment is
appropriate is based on the felony
convictions referenced herein. The
factual basis for these convictions is as
follows: Mr. Soto was a registered nurse
working for Ideal Home Health Inc.
(Ideal), which was a business in MiamiDade County, FL. Ideal purportedly
provided skilled nursing services to
Medicare beneficiaries who required
home health services. As a registered
nurse in the home health field, it was
Mr. Soto’s duty to provide skilled
nursing services to patients and
maintain proper documentation of all
treatments provided to patients.
Mr. Soto conspired with others to
defraud Medicare. Mr. Soto and his
coconspirators, among other things,
submitted and caused the submission of
false and fraudulent claims to Medicare
and concealed the submission of these
false and fraudulent claims.
Mr. Soto and his co-conspirators
falsified and caused Medicare
beneficiaries to falsify weekly visit/time
record sheets, falsified skilled nursing
progress notes representing that Mr.
Soto had administered insulin
injections and provided various other
medical services to Medicare
beneficiaries, and caused Ideal to
submit false and fraudulent claims to
Medicare for home health benefits by
falsely representing that they had
provided these home health services. As
a result of these fraudulent claims, Mr.
Soto caused Medicare to make payments
E:\FR\FM\20OCN1.SGM
20OCN1
tkelley on DSK3SPTVN1PROD with NOTICES
Federal Register / Vol. 79, No. 202 / Monday, October 20, 2014 / Notices
to Ideal, which amounted to
approximately $58,400.
As a result of his conviction on April
9, 2014, FDA sent Mr. Soto a notice by
certified mail proposing to debar him
for 6 years from providing services in
any capacity to a person that has an
approved or pending drug product
application. The proposal was based on
a finding under section
306(b)(2)(B)(ii)(I) of the FD&C Act that
Mr. Soto was convicted of felonies
under Federal law for conduct which
involved health care fraud, and the
Agency found, on the basis of the
conviction and other information, that
Mr. Soto had demonstrated a pattern of
conduct sufficient to find that there is
reason to believe he may violate
requirements under the FD&C Act
relating to drug products. This
conclusion was based on the fact that
Mr. Soto had legal and professional
obligations to ensure that he submitted
accurate medical claims for services he
provided, as well as ensure that he
provided the appropriate drug products
to his patients. Instead, Mr. Soto
submitted and caused the submission of
false weekly visit/time record sheets
and false daily blood sugar/insulin log
sheets. He engaged in this conduct
repeatedly over a period of more than 2
years. His convictions indicate that he
knowingly and willfully disregarded his
legal and professional obligations to
keep accurate medical records and to
submit accurate claims for the services
he provided. Having considered the
conduct that forms the basis of his
conviction and the fact that this conduct
occurred in the course of his profession
and showed a disregard for the
obligations of his profession and the
law, FDA found that Mr. Soto has
demonstrated a pattern of conduct
sufficient to find that there is reason to
believe that, if he were to provide
services to a person that has an
approved or pending drug application,
he may violate requirements under the
FD&C Act relating to drug products.
Therefore, FDA had reason to believe
that, if Mr. Soto were to provide services
to a person that has an approved or
pending drug application, he may
violate requirements under the FD&C
Act relating to drug products.
The proposal offered Mr. Soto an
opportunity to request a hearing,
providing him with 30 days from the
date of receipt of the letter in which to
file the request, and advised him that
failure to request a hearing constituted
a waiver of the opportunity for a hearing
and of any contentions concerning this
action. The proposal was received on
April 14, 2014. Mr. Soto failed to
respond within the timeframe
VerDate Sep<11>2014
16:28 Oct 17, 2014
Jkt 235001
prescribed by regulation and has,
therefore, waived his opportunity for a
hearing and has waived any contentions
concerning his debarment (21 CFR part
12).
II. Findings and Order
Therefore, the Director, Office of
Enforcement and Import Operations,
Office of Regulatory Affairs, under
section 306(b)(2)(B)(ii)(I) of the FD&C
Act, under authority delegated to the
Director (Staff Manual Guide 1410.35),
finds that Kelvin Soto has been
convicted of four counts of a felony and
one count of conspiracy to commit a
felony under Federal law for conduct
involving health care fraud, and on the
basis of the conviction and other
information, finds that Mr. Soto has
demonstrated a pattern of conduct
sufficient to find that there is reason to
believe he may violate requirements
under the FD&C Act relating to drug
products.
Based on the factors under section
306(c)(2)(A)(iii) of the FD&C Act (21
U.S.C. 335a(c)(2)(A)(iii)), FDA finds that
each offense be accorded a debarment
period of 3 years. In the case of a person
debarred for multiple offenses, FDA
shall determine whether the periods of
debarment shall run concurrently or
consecutively (21 U.S.C. 335a(c)(2)(A)).
FDA has concluded that the 3-year
period of debarment for each of the five
offenses of conviction need not be
served consecutively. Rather, FDA has
concluded that the 3-year periods of
debarment for the four counts of health
care fraud shall run concurrently. The 3year period of debarment for the
conspiracy conviction shall run
consecutively to the periods of
debarment for the health care fraud
convictions, resulting in a total
debarment period of 6 years.
As a result of the foregoing finding,
Kelvin Soto is debarred for a period of
6 years from providing services in any
capacity to a person with an approved
or pending drug product application
under sections 505, 512, or 802 of the
FD&C Act (21 U.S.C. 355, 360b, or 382),
or under section 351 of the Public
Health Service Act (42 U.S.C. 262),
effective (see DATES) (see sections
201(dd), 306(c)(1)(B), and
306(c)(2)(A)(ii) of the FD&C Act (21
U.S.C. 321(dd), 335a(c)(1)(B), and
335a(c)(2)(A)(ii)). Any person with an
approved or pending drug product
application who knowingly employs or
retains Mr. Soto as a consultant or
contractor, or otherwise uses the
services of Kelvin Soto in any capacity
during his debarment, will be subject to
civil money penalties (section 307(a)(6)
of the FD&C Act (21 U.S.C. 335b(a)(6))).
PO 00000
Frm 00043
Fmt 4703
Sfmt 4703
62635
In addition, FDA will not accept or
review any abbreviated new drug
applications submitted by or with the
assistance of Kelvin Soto during his
period of debarment (section
306(c)(l)(A) of the FD&C Act).
Any application by Mr. Soto for
termination of debarment under section
306(d)(4) of the FD&C Act should be
identified with Docket No. FDA–2013–
N–0960 and sent to the Division of
Dockets Management (see ADDRESSES).
All such submissions are to be filed in
four copies. The public availability of
information in these submissions is
governed by 21 CFR 10.20(j).
Publicly available submissions may
be seen in the Division of Dockets
Management between 9 a.m. and 4 p.m.,
Monday through Friday.
Dated: October 14, 2014.
Leslie Kux,
Assistant Commissioner for Policy.
[FR Doc. 2014–24814 Filed 10–17–14; 8:45 am]
BILLING CODE 4164–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2014–D–1492]
Two-Phased Chemistry,
Manufacturing, and Controls Technical
Sections; Draft Guidance for Industry;
Availability
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Notice.
The Food and Drug
Administration (FDA) is announcing the
availability of a draft guidance for
industry (GFI #227) entitled ‘‘TwoPhased Chemistry, Manufacturing, and
Controls (CMC) Technical Sections.’’
The purpose of this document is to
provide recommendations to sponsors
submitting CMC data submissions. For
review efficiency, the Center for
Veterinary Medicine (CVM) prefers that
CMC information be submitted in a
single technical section. However, there
may be instances when a two-phased
technical submission process is more
beneficial to improve the overall time to
drug approval. Sponsors may submit the
phased CMC technical section as a
single technical section or a two-phased
technical section. This guidance
describes the use of the two-phased
technical section submission process.
DATES: Although you can comment on
any guidance at any time (see 21 CFR
10.115(g)(5)), to ensure that the Agency
considers your comment on this draft
SUMMARY:
E:\FR\FM\20OCN1.SGM
20OCN1
Agencies
[Federal Register Volume 79, Number 202 (Monday, October 20, 2014)]
[Notices]
[Pages 62634-62635]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2014-24814]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA-2013-N-0960]
Kelvin Soto: Debarment Order
AGENCY: Food and Drug Administration, HHS.
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: The Food and Drug Administration (FDA) is issuing an order
under the Federal Food, Drug, and Cosmetic Act (the FD&C Act) debarring
Kelvin Soto from providing services in any capacity to a person that
has an approved or pending drug product application for a period of 6
years. We base this order on a finding that Mr. Soto was convicted of
four felony counts under Federal law for conduct involving health care
fraud and conspiracy to commit health care fraud and that this pattern
of conduct is sufficient to find that there is reason to believe he may
violate requirements under the FD&C Act relating to drug products. Mr.
Soto was given notice of the proposed debarment and an opportunity to
request a hearing within the timeframe prescribed by regulation. Mr.
Soto failed to request a hearing. Mr. Soto's failure to request a
hearing constitutes a waiver of his right to a hearing concerning this
action.
DATES: This order is effective October 20, 2014.
ADDRESSES: Submit applications for termination of debarment to the
Division of Dockets Management (HFA-305), Food and Drug Administration,
5630 Fishers Lane, Rm. 1061, Rockville, MD 20852.
FOR FURTHER INFORMATION CONTACT: Kenny Shade, Office of Regulatory
Affairs, Food and Drug Administration, 12420 Parklawn Dr., Element
Bldg., Rm. 4144, Rockville, MD 20857, 301-796-4640.
SUPPLEMENTARY INFORMATION:
I. Background
Section 306(b)(2)(B)(ii)(I) of the FD&C Act (21 U.S.C.
335a(b)(2)(B)(ii)(I)) permits debarment of an individual if FDA finds
that the individual has been convicted of a felony under Federal law
for conduct that involves bribery; payment of illegal gratuities;
fraud; perjury; false statement; racketeering; blackmail; extortion;
falsification or destruction of records; interference with, obstruction
of an investigation into, or prosecution of any criminal offense; and
FDA finds, on the basis of the conviction and other information, that
such individual has demonstrated a pattern of conduct sufficient to
find that there is reason to believe the individual may violate
requirements under the FD&C Act relating to drug products.
On November 6, 2012, the U.S. District Court for the Southern
District of Florida entered judgment against Mr. Soto after a jury
found him guilty of four counts of health care fraud in violation of 18
U.S.C. 1347 and one count of conspiracy to commit health care fraud in
violation of 18 U.S.C. 1349.
FDA's finding that debarment is appropriate is based on the felony
convictions referenced herein. The factual basis for these convictions
is as follows: Mr. Soto was a registered nurse working for Ideal Home
Health Inc. (Ideal), which was a business in Miami-Dade County, FL.
Ideal purportedly provided skilled nursing services to Medicare
beneficiaries who required home health services. As a registered nurse
in the home health field, it was Mr. Soto's duty to provide skilled
nursing services to patients and maintain proper documentation of all
treatments provided to patients.
Mr. Soto conspired with others to defraud Medicare. Mr. Soto and
his coconspirators, among other things, submitted and caused the
submission of false and fraudulent claims to Medicare and concealed the
submission of these false and fraudulent claims.
Mr. Soto and his co-conspirators falsified and caused Medicare
beneficiaries to falsify weekly visit/time record sheets, falsified
skilled nursing progress notes representing that Mr. Soto had
administered insulin injections and provided various other medical
services to Medicare beneficiaries, and caused Ideal to submit false
and fraudulent claims to Medicare for home health benefits by falsely
representing that they had provided these home health services. As a
result of these fraudulent claims, Mr. Soto caused Medicare to make
payments
[[Page 62635]]
to Ideal, which amounted to approximately $58,400.
As a result of his conviction on April 9, 2014, FDA sent Mr. Soto a
notice by certified mail proposing to debar him for 6 years from
providing services in any capacity to a person that has an approved or
pending drug product application. The proposal was based on a finding
under section 306(b)(2)(B)(ii)(I) of the FD&C Act that Mr. Soto was
convicted of felonies under Federal law for conduct which involved
health care fraud, and the Agency found, on the basis of the conviction
and other information, that Mr. Soto had demonstrated a pattern of
conduct sufficient to find that there is reason to believe he may
violate requirements under the FD&C Act relating to drug products. This
conclusion was based on the fact that Mr. Soto had legal and
professional obligations to ensure that he submitted accurate medical
claims for services he provided, as well as ensure that he provided the
appropriate drug products to his patients. Instead, Mr. Soto submitted
and caused the submission of false weekly visit/time record sheets and
false daily blood sugar/insulin log sheets. He engaged in this conduct
repeatedly over a period of more than 2 years. His convictions indicate
that he knowingly and willfully disregarded his legal and professional
obligations to keep accurate medical records and to submit accurate
claims for the services he provided. Having considered the conduct that
forms the basis of his conviction and the fact that this conduct
occurred in the course of his profession and showed a disregard for the
obligations of his profession and the law, FDA found that Mr. Soto has
demonstrated a pattern of conduct sufficient to find that there is
reason to believe that, if he were to provide services to a person that
has an approved or pending drug application, he may violate
requirements under the FD&C Act relating to drug products. Therefore,
FDA had reason to believe that, if Mr. Soto were to provide services to
a person that has an approved or pending drug application, he may
violate requirements under the FD&C Act relating to drug products.
The proposal offered Mr. Soto an opportunity to request a hearing,
providing him with 30 days from the date of receipt of the letter in
which to file the request, and advised him that failure to request a
hearing constituted a waiver of the opportunity for a hearing and of
any contentions concerning this action. The proposal was received on
April 14, 2014. Mr. Soto failed to respond within the timeframe
prescribed by regulation and has, therefore, waived his opportunity for
a hearing and has waived any contentions concerning his debarment (21
CFR part 12).
II. Findings and Order
Therefore, the Director, Office of Enforcement and Import
Operations, Office of Regulatory Affairs, under section
306(b)(2)(B)(ii)(I) of the FD&C Act, under authority delegated to the
Director (Staff Manual Guide 1410.35), finds that Kelvin Soto has been
convicted of four counts of a felony and one count of conspiracy to
commit a felony under Federal law for conduct involving health care
fraud, and on the basis of the conviction and other information, finds
that Mr. Soto has demonstrated a pattern of conduct sufficient to find
that there is reason to believe he may violate requirements under the
FD&C Act relating to drug products.
Based on the factors under section 306(c)(2)(A)(iii) of the FD&C
Act (21 U.S.C. 335a(c)(2)(A)(iii)), FDA finds that each offense be
accorded a debarment period of 3 years. In the case of a person
debarred for multiple offenses, FDA shall determine whether the periods
of debarment shall run concurrently or consecutively (21 U.S.C.
335a(c)(2)(A)). FDA has concluded that the 3-year period of debarment
for each of the five offenses of conviction need not be served
consecutively. Rather, FDA has concluded that the 3-year periods of
debarment for the four counts of health care fraud shall run
concurrently. The 3-year period of debarment for the conspiracy
conviction shall run consecutively to the periods of debarment for the
health care fraud convictions, resulting in a total debarment period of
6 years.
As a result of the foregoing finding, Kelvin Soto is debarred for a
period of 6 years from providing services in any capacity to a person
with an approved or pending drug product application under sections
505, 512, or 802 of the FD&C Act (21 U.S.C. 355, 360b, or 382), or
under section 351 of the Public Health Service Act (42 U.S.C. 262),
effective (see DATES) (see sections 201(dd), 306(c)(1)(B), and
306(c)(2)(A)(ii) of the FD&C Act (21 U.S.C. 321(dd), 335a(c)(1)(B), and
335a(c)(2)(A)(ii)). Any person with an approved or pending drug product
application who knowingly employs or retains Mr. Soto as a consultant
or contractor, or otherwise uses the services of Kelvin Soto in any
capacity during his debarment, will be subject to civil money penalties
(section 307(a)(6) of the FD&C Act (21 U.S.C. 335b(a)(6))). In
addition, FDA will not accept or review any abbreviated new drug
applications submitted by or with the assistance of Kelvin Soto during
his period of debarment (section 306(c)(l)(A) of the FD&C Act).
Any application by Mr. Soto for termination of debarment under
section 306(d)(4) of the FD&C Act should be identified with Docket No.
FDA-2013-N-0960 and sent to the Division of Dockets Management (see
ADDRESSES). All such submissions are to be filed in four copies. The
public availability of information in these submissions is governed by
21 CFR 10.20(j).
Publicly available submissions may be seen in the Division of
Dockets Management between 9 a.m. and 4 p.m., Monday through Friday.
Dated: October 14, 2014.
Leslie Kux,
Assistant Commissioner for Policy.
[FR Doc. 2014-24814 Filed 10-17-14; 8:45 am]
BILLING CODE 4164-01-P