Nasim F. Khan, M.D.; Denial of Application, 4630-4633 [E8-1241]
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Federal Register / Vol. 73, No. 17 / Friday, January 25, 2008 / Notices
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permits at its East Liverpool facility; (4)
certify that it does not currently process
nonmetallic minerals at its East
Liverpool facility, and in the event that
it resumes such processing, comply
with applicable provisions of NSPS;
and, implement two Supplemental
Environmental Projects valued at
$386,592, consisting of a Truck Loadout
Shed and Road Paving Projects at its
East Liverpool facility.
The Department of Justice will
receive, for a period of thirty (30) days
from the date of this publication,
comments relating to the proposed
Consent Decree. Comments should be
addressed to the Assistant Attorney
General, Environment and Natural
Resources Division, and either emailed
to pubcomment-ees.enrd@usdoj.gov or
mailed to United States Department of
Justice, P.O. Box 7611, Washington, DC
20044–7611, and should refer to United
States v. S.H. Bell Co., Civil No. 4:08–
cv–96 (N.D. Ohio), and DOJ Reference
No. 90–5–2–1–07823.
The proposed Consent Decree may be
examined at: (1) The Office of the
United States Attorney for the Northern
District of Ohio, 801 West Superior
Avenue, Suite 400, Cleveland, OH,
44113 (216–622–3600); and (2) the
United States Environmental Protection
Agency (Region 5), 77 West Jackson
Blvd., Chicago, IL 60604–3507 (contact:
John C. Matson (312–886–2243).
During the public comment period,
the proposed Consent Decree may also
be examined on the following U.S.
Department of Justice Web site,
https://www.usdoj.gov/enrd/
Consent_Decrees.html. A copy of the
proposed Consent Decree may also be
obtained by mail from the Consent
Decree Library, U.S. Department of
Justice, P.O. Box 7611, Washington, DC
20044–7611 or by faxing or e-mailing a
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pages), made payable to the U.S.
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a check in that amount to the Consent
Decree Library at the stated address.
William D. Brighton,
Assistant Chief, Environmental Enforcement
Section, Environment and Natural Resources
Division.
[FR Doc. 08–271 Filed 1–24–08: 8:45 am]
BILLING CODE 4410–15–M
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DEPARTMENT OF JUSTICE
in the amount of $36.50 ($.25 per page)
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Notice of Lodging Consent Decree
Pursuant to the Clean Air Act, the
Comprehensive Environmental
Response, Compensation and Liability
Act, and the Emergency Planning and
Community Right-To-Know Act
Robert D. Brook,
Assistant Chief, Environmental Enforcement
Section, Environment and Natural Resources
Division.
[FR Doc. 08–265 Filed 1–24–08; 8:45 am]
In accordance with 28 CFR 50.7,
notice is hereby given that on January
15, 2008, a proposed consent decree in
United States v. Sinclair Wyoming
Refining Co., et al., Case No. 08cv020–
D, was lodged with the United States
Court for the District of Wyoming. The
proposed consent decree would resolve
the United States’ claims against
Sinclair Wyoming. Refining Company,
Sinclair Casper Refining Company, and
Sinclair Tulsa Refining Company
(collectively the ‘‘Sinclair Refineries’’)
brought pursuant to Section 113(b) of
the CAA, 42 U.S.C. 7413(b); Section
103(a) of the Comprehensive
Environmental Response, Compensation
and Liability Act, 42 U.S.C. 9603(a); and
Section 304 of the Emergency Planning
and Community Right-To-Know Act, 42
U.S.C. 11004. Under the terms of the
consent decree, the Sinclair Refineries
will pay civil penalties totaling
$2,450,000 to the United States and the
states of Oklahoma and Wyoming,
undertake supplemental environmental
projects valued at $150,000, and
complete extensive injunctive relief.
The Department of Justice will receive
comments relating to the proposed
consent decree for a period of thirty (30)
days from the date of this publication.
Comments should be addressed to the
Assistant Attorney General,
Environment and Natural Resources
Division, P.O. Box 7611, U.S.
Department of Justice, Washington, DC
20044–7611, and may be submitted
electronic mail to the following address:
pubcomment-ees.enrd@usdoj.gov.
Comments should refer to United States
v. Sinclair Wyoming Refining Co., et al.,
Case No. 08cv020–D, and Department of
Justice Reference No. 90–5–2–1–07793.
The consent decree may be examined
on the following Department of Justice
Web site, https://www.usdoj.gov/enrd/
Consent_Decrees.html. A copy of the
consent decree may also be obtained by
mail from the Consent Decree Library,
P.O. Box 7611, U.S. Department of
Justice, Washington, DC 20044–7611 or
by faxing or e-mailing a request to Tonia
Fleetwood (tonia.fleetwood@usdoj.gov),
fax no. (202) 514–0097, phone
confirmation number (202) 514–1547. In
requesting a copy from the Consent
Decree Library, please enclose a check
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BILLING CODE 4410–15–M
DEPARTMENT OF JUSTICE
Drug Enforcement Administration
Nasim F. Khan, M.D.; Denial of
Application
On June 8, 2007, the Deputy Assistant
Administrator, Office of Diversion
Control, Drug Enforcement
Administration, issued an Order to
Show Cause to Nasim F. Khan, M.D.
(Respondent), of Houston, Texas. The
Show Cause Order proposed the denial
of Respondent’s pending application for
a DEA Certificate of Registration as a
practitioner on two grounds: (1) That
she lacked authority under state law to
handle controlled substances, and (2)
that her ‘‘registration would be
inconsistent with the public interest.’’
Show Cause Order at 1; see also 21
U.S.C. 823(f).
The Show Cause Order specifically
alleged that ‘‘[o]n June 26, 2006,
[Respondent’s] Texas Controlled
Substance Registration was terminated,’’
and that she was therefore ‘‘not
currently authorized by the State of
Texas to prescribe, dispense, or
otherwise handle controlled
substances.’’ Show Cause Order at 1.
The Show Cause Order further alleged
that Respondent had committed acts
inconsistent with the public interest
because she had ‘‘allowed [her] DEA
registration to be used to dispense
controlled substances for other than
legitimate medical purposes’’ and had
‘‘engage[ed] in self-prescribing of
controlled substances, in violation of
the Texas Controlled Substances Act.’’
Id.
On June 15, 2007, the Show Cause
Order, which also notified Respondent
of her right to request a hearing on the
allegations, was served on Respondent
by Federal Express delivered to her
residence. Because: (1) More than thirty
days have passed since service of the
Show Cause Order, and (2) neither
Respondent, nor anyone purporting to
represent her, has requested a hearing,
I conclude that Respondent has waived
her right to a hearing. See 21 CFR
1301.43(d). I therefore enter this Final
Order without a hearing based on
relevant material contained in the
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investigative file, see id. 1301.43(e), and
make the following findings.
jlentini on PROD1PC65 with NOTICES
Findings
Respondent is a physician with a
specialty in psychiatry and pathology.
Respondent previously held a DEA
Certificate of Registration as a
practitioner at the registered location of
Houston Medical Clinic, 10881
Richmond Ave., Apt. 412, Houston,
Texas. In July 2004, DEA Diversion
Investigators with the Houston Field
Division received information that
Respondent was prescribing
promethazine with codeine cough
syrup, a schedule V controlled
substance, see 21 CRR 1308.15(c), to an
individual who had been arrested three
times by the Houston Police Department
for unlawfully possessing controlled
substances.
In August 2005, DEA Diversion
Investigators (DIs) received information
that two unlicensed individuals (F.K.
and V.V.), who worked at the Main
Medical Clinic (which was located in
Jacinto City, Texas), were using
Respondent’s DEA registration to issue
controlled-substance prescriptions for
drugs which included Lorcet 10/650 (a
branded drug combining hydrocodone
and acetaminophen and a schedule III
controlled substance, see 21 CFR
1308.13(e), Xanax (alprazolam), a
schedule IV controlled substance, see
id. 1308.14(c), and promethazine with
codeine cough syrup. Id. 1308.15(c).
F.K. and V.V. charged $100 for each
prescription.
The DIs subsequently went to the
clinic and interviewed several people.
While the DIs were told that Respondent
had terminated her employment at the
clinic, they also obtained a stack of
prescription carbons. The copies
indicated the patient’s name, the name
of a controlled substance, and
Respondent’s DEA number. During
other interviews, the DIs determined
that Respondent had seen only one or
two ‘‘patients’’ each day, and that most
of the clinic’s ‘‘patients’’ were seen by
other people including several foreign
graduate students who were not
licensed in any field of medical
practice. The DIs also confirmed that
V.V. had sold a stack of prescriptions,
which bore a signature similar to
Respondent’s, for a large amount of
cash.
Thereafter, on August 11, 2005, the
DIs interviewed Respondent at the
location of a clinic (named the ‘‘45
Clinic’’) which she was opening in
Houston and for which she needed to
change the address of her registered
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location.1 During the interview,
Respondent stated that she had seen
approximately forty patients a day at the
Main Medical Clinic and that the cost
for a controlled-substance prescription
was $80 cash. Respondent further stated
that at the clinic, foreign graduate
students worked under her supervision
and wrote the prescriptions which she
then signed. Respondent also stated that
she had taken a continuing medical
education class in pain management
and that the only controlled substances
she prescribed were Vicodin, Lorcet,
and Lortab.2
In the course of the investigation, the
DIs had previously determined that
Respondent had obtained controlled
substances based on 117 prescriptions
issued to her under her DEA number.
During the interview, Respondent
denied that she had self-prescribed and
claimed that her son was also a
physician and had prescribed the
controlled substances for her.
Subsequently, the DIs searched the
Texas Medical Board’s website and
found that there was no listing for her
son.
The DIs had also previously
determined that between January 1,
2004, and August 11, 2005, Respondent
had obtained approximately 474 twentyfive ml. bottles of schedule V cough
medicines. When asked as to why she
had ordered the drugs, Respondent
maintained that they were small
containers of cough syrup which she
used when she was unable to sleep.
While at Respondent’s new clinic, the
DIs interviewed V.V., the same
individual who had been implicated in
selling controlled-substance
prescriptions at Respondent’s former
employer. V.V. told the investigators
that she had first met Respondent on
that very day (when she had
purportedly interviewed for a position
at the clinic) and that her duties at
Respondent’s clinic would include
scheduling appointments, taking vital
signs, and other duties performed by
receptionists.
Thereafter, on August 30, 2005, a
registration technician changed
Respondent’s registered location to the
address of her new clinic.
Approximately three weeks later, on
September 19, 2005, Respondent
notified a DI that V.V. was using her
DEA number to write unauthorized
prescriptions for unknown individuals.
Later that day, two DIs interviewed
Respondent at her residence.
1 According to the investigative file, Respondent
did not own the clinic.
2 Respondent also stated that she prescribed
Ritalin for her child psychiatric patients who had
Attention Deficit Disorder.
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Respondent told the DIs that she had
terminated her employment at the Main
Medical Clinic because she suspected
that its owner was involved in illegal
activities. Respondent stated that she
had contacted DEA because she had
received information that the Corpus
Christi, Texas Police Department was
looking for her regarding prescriptions
she had written. Respondent further
stated that during the previous week,
she had gone to her new clinic and
attempted to retrieve her prescriptions
but was told that the pads belonged to
the clinic. Respondent added that she
had become concerned that someone
was using her DEA number to issue
prescriptions without her consent.
Because of the unauthorized use of her
number, Respondent then agreed to
voluntarily surrender her DEA
registration. She also surrendered her
state controlled-substances registration.
On September 30, 2005, Respondent
applied for a new registration using the
address of the 45 Clinic for her
proposed registered location. Several
days later, two DIs went to Respondent’s
residence and attempted to interview
her. Upon opening the door,
Respondent started screaming at the DIs
and stated that they should contact her
attorney. When one of the DIs asked
Respondent for her attorney’s phone
number, Respondent stated that she
would get the number and slammed the
door. Several minutes later, Respondent
opened the door, threw a piece of paper
at the DI, and stated in a loud voice that
‘‘the White House knew who her father
was and that she was his daughter.’’
After the DIs told Respondent that they
were there to speak to her about her
application, Respondent stated that
‘‘there would be no trick or treating here
today.’’ One of the DIs again asked
Respondent whether she had applied for
a new registration. Respondent
answered ‘‘yes’’ and again slammed the
door shut.
Thereafter, a local pharmacist notified
DEA investigators that on October 3 and
4, he had received two prescriptions
which were written under Respondent’s
DEA number. The pharmacist told the
DIs that when he had attempted to
verify one the prescriptions, Respondent
did not return the call. Respondent, in
a subsequent interview, denied issuing
the prescriptions.
On January 5, 2006, a detective with
the Garland, Texas Police Department
notified one of the DIs that numerous
prescriptions written under
Respondent’s former DEA registration
had been presented at a local pharmacy.
The prescriptions bore the name and
address of the Main Medical Clinic,
Respondent’s former employer.
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Thereafter, on March 28, 2006, an
official of the Texas Department of
Public Safety (DPS) notified a DI that
the State intended to terminate
Respondent’s state controlledsubstances registration. The state official
further told the DI that Respondent’s
application had been erroneously
granted because at the time the
application was approved, the State was
upgrading its computer system and was
unable to access her history.
Subsequently, on June 26, 2006, DPS
terminated Respondent’s state
controlled-substances registration on the
ground that she was prohibited under
the State’s rules for re-applying for a
period of one year following her
surrendering of her state registration. I
further find that the State has not reinstated her controlled-substances
registration.
I also find that on August 24, 2007,
Respondent entered into an Agreed
Order with the Texas Medical Board.
Under the order, Respondent
voluntarily and permanently
surrendered her medical license.
According to the Texas Medical Board’s
website, ‘‘[t]he action was based on
[Respondent’s] failure to meet the
standard of care due [to] her nontherapeutic prescription of controlled
substances to four patients and to
herself.’’
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Discussion
Section 303(f) of the Controlled
Substances Act provides that ‘‘[t]he
Attorney General shall register
practitioners * * * to dispense * * *
controlled substances in schedule II, III,
IV, or V, if the applicant is authorized
to dispense * * * controlled substances
under the laws of the State in which he
practices.’’ 21 U.S.C. 823(f). Section
303(f) further provides that ‘‘[t]he
Attorney General may deny an
application for such registration if he
determines that the issuance of such
registration would be inconsistent with
the public interest.’’ Id. In making the
public interest determination, the Act
requires the consideration of the
following factors:
(1) The recommendation of the appropriate
State licensing board or professional
disciplinary authority.
(2) The applicant’s experience in
dispensing * * * controlled substances.
(3) The applicant’s conviction record under
Federal or State laws relating to the
manufacture, distribution, or dispensing of
controlled substances.
(4) Compliance with applicable State,
Federal, or local laws relating to controlled
substances.
(5) Such other conduct which may threaten
the public health and safety.
Id.
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‘‘[T]hese factors are * * * considered
in the disjunctive.’’ Robert A. Leslie,
M.D., 68 FR 15227, 15230 (2003). I ‘‘may
rely on any one or a combination of
factors, and may give each factor the
weight [I] deem[] appropriate in
determining whether a registration
should be revoked.’’ Id. Moreover, I am
‘‘not required to make findings as to all
of the factors.’’ Hoxie v. DEA, 419 F.3d
477, 482 (6th Cir. 2005); see also Morall
v. DEA, 412 F.3d 165, 173–74 (DC Cir.
2005).
In this case, I conclude that there are
two independent grounds for denying
Respondent’s application. First,
Respondent is not currently authorized
under Texas law to handle controlled
substances and thus does not meet an
essential requirement for a registration
under the CSA. Second, while it appears
that Respondent will not be returning to
medical practice anytime soon, her
experience in dispensing controlled
substances and her record of
compliance with applicable laws make
clear that granting her a registration
‘‘would be inconsistent with the public
interest.’’ 21 U.S.C. 823(f).
Under the Controlled Substances Act
(CSA), a practitioner must be currently
authorized to handle controlled
substances in ‘‘the jurisdiction in which
[she] practices’’ in order to maintain a
DEA registration. See 21 U.S.C. 802(21)
(‘‘[t]he term ‘practitioner’ means a
physician * * * licensed, registered, or
otherwise permitted, by * * * the
jurisdiction in which he practices * * *
to distribute, dispense, [or] administer
* * * a controlled substance in the
course of professional practice’’). See
also id. section 823(f) (‘‘The Attorney
General shall register practitioners
* * * if the applicant is authorized to
dispense * * * controlled substances
under the laws of the State in which he
practices.’’). Relatedly, DEA has
repeatedly held that the CSA requires
the revocation of a registration issued to
a practitioner who no longer possesses
authority under state law to handle
controlled substances. See Sheran
Arden Yeates, 71 FR 39130, 39131
(2006); Dominick A. Ricci, 58 FR 51104,
51105 (1993); Bobby Watts, 53 FR
11919, 11920 (1988). See also 21 U.S.C.
824(a)(3) (authorizing the revocation of
a registration ‘‘upon a finding that the
registrant * * * has had his State
license or registration suspended [or]
revoked * * * and is no longer
authorized by State law to engage in the
* * * distribution [or] dispensing of
controlled substances’’).
Here, the investigative file establishes
that Respondent’s Texas controlledsubstances registration was terminated
on June 26, 2006. Moreover, there is no
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evidence that the State has issued a new
controlled substance registration to her,
and the Agreed Order which
Respondent entered into with the Texas
Medical Board suggests that the State
will not grant her a new controlledsubstances registration any time soon.
Because Respondent is without
authority to handle controlled
substances in Texas, the State in which
she seeks a DEA registration, she does
not meet an essential prerequisite for a
new DEA registration. Accordingly, her
application is denied on that basis. See
21 U.S.C. 823(f).
I further note that even if Respondent
possessed a state registration, the record
would still support the denial of her
application on the ground that her
registration would be ‘‘inconsistent with
the public interest.’’ 21 U.S.C. 823(f). As
the State found, Respondent has
engaged in the non-therapeutic
prescription of controlled substances
both to herself and others.
With respect to her self-prescribing,
the record establishes that Respondent
issued to herself 117 prescriptions for
narcotic-cough syrups, which are
schedule V controlled substances. The
record further establishes that
Respondent’s statements to investigators
that the prescriptions were issued to her
by her son, and that her son was a
physician, were false.
Moreover, there is also substantial
and disturbing evidence that
Respondent failed to exercise proper
control over her prescriptions pads and
allowed unlicensed and un-registered
individuals at the Main Medical Clinic
to write prescriptions under her DEA
registration. This conduct violates
federal law and regulations, which
require that a prescription be ‘‘issued for
a legitimate medical purpose by an
individual practitioner acting in the
usual course of [her] professional
practice,’’ 21 CFR 1306.04(a), and that
each person writing a prescription be
‘‘[a]uthorized to prescribe controlled
substances by the jurisdiction in which
he is licensed to practice his profession
and * * * [e]ither registered or
exempted from registration.’’ Id.
§ 1306.03(a). Accordingly, even if
Respondent held a state registration, her
abysmal experience in dispensing
controlled substances and her record of
non-compliance with federal and state
laws related to controlled substances
would nonetheless require the denial of
her application.
Order
Pursuant to the authority vested in me
by 21 U.S.C. 823(f), as well as 28 CFR
0.100(b) & 0.104, I order that the
application of Nasim F. Khan, M.D., for
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a DEA Certificate of Registration as a
practitioner be, and it hereby is, denied.
This order is effective February 25,
2008.
Dated: January 17, 2008.
Michele M. Leonhart,
Deputy Administrator.
[FR Doc. E8–1241 Filed 1–24–08; 8:45 am]
BILLING CODE 4410–09–P
DEPARTMENT OF LABOR
Office of the Secretary
Submission for OMB Review:
Comment Request
jlentini on PROD1PC65 with NOTICES
January 18, 2008.
The Department of Labor (DOL)
hereby announces the submission of the
following public information collection
requests (ICR) to the Office of
Management and Budget (OMB) for
review and approval in accordance with
the Paperwork Reduction Act of 1995
(Pub. L. 104–13, 44 U.S.C. chapter 35).
A copy of each ICR, with applicable
supporting documentation; including
among other things a description of the
likely respondents, proposed frequency
of response, and estimated total burden
may be obtained from the RegInfo.gov
Web site at https://www.reginfo.gov/
public/do/PRAMain or by contacting
Darrin King on 202–693–4129 (this is
not a toll-free number)/e-mail:
king.darrin@dol.gov.
Interested parties are encouraged to
send comments to the Office of
Information and Regulatory Affairs,
Attn: Bridget Dooling, OMB Desk
Officer for the Employment Standards
Administration (ESA), Office of
Management and Budget, Room 10235,
Washington, DC 20503, Telephone:
202–395–7316/Fax: 202–395–6974
(these are not toll-free numbers), E-mail:
OIRA_submission@omb.eop.gov within
30 days from the date of this publication
in the Federal Register. In order to
ensure the appropriate consideration,
comments should reference the OMB
Control Number (see below).
The OMB is particularly interested in
comments which:
• 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;
• Evaluate the accuracy of the
agency’s estimate of the burden of the
proposed collection of information,
including the validity of the
methodology and assumptions used;
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• Enhance the quality, utility, and
clarity of the information to be
collected; and
• 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.
Agency: Employment Standards
Administration.
Type of Review: Extension without
change of currently approved collection.
Title: Certification of Funeral
Expenses.
OMB Control Number: 1215–0027.
Form Number: LS–265.
Estimated Number of Respondents:
195.
Total Estimated Annual Burden
Hours: 49.
Total Estimated Cost Burden: $86.
Affected Public: Private Sector:
Business or other for-profits.
Description: The Form LS–265 is used
to report funeral expenses payable
under section 9(a) of the Longshore and
Harbor Workers’ Act [ 33 U.S.C. 909].
Agency: Employment Standards
Administration.
Type of Review: Revision of currently
approved collection.
Title: Comparability of Current Work
to Coal Mine Employment.
OMB Control Number: 1215–0056.
Form Numbers: CM–913 (the Forms
CM–918 and CM–1093 are being
discontinued).
Estimated Number of Respondents:
1,350.
Total Estimated Annual Burden
Hours: 675.
Total Estimated Cost Burden: $594.
Affected Public: Individuals or
households.
Description: Once a miner has been
identified as having performed non-coal
mine work subsequent to coal mine
employment, the miner or the miner’s
survivor is asked to complete a Form
CM–913. The Form is used to compare
the physical demands of the miner’s
coal mine work with last or current noncoal mine work. This employment
information, together with medical
information, is used to establish
whether the miner is totally disabled
due to black lung disease caused by coal
mine employment, a criterion for
entitlement of benefits. Information
collected on the Form CM–913 helps
DOL to determine if the miner has or
had a reduced ability to perform his
usual and customary coal mine work.
The Black Lung Benefits Act, as
amended, 30 U.S.C. 901 et. seq. and 20
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4633
CFR 718.204(b)(1) necessitate the
collection of this information.
Darrin A. King,
Acting Departmental Clearance Officer.
[FR Doc. E8–1291 Filed 1–24–08; 8:45 am]
BILLING CODE 4510–CK–P
DEPARTMENT OF LABOR
Employment and Training
Administration
Notice of Determinations Regarding
Eligibility To Apply for Worker
Adjustment Assistance and Alternative
Trade Adjustment Assistance
In accordance with Section 223 of the
Trade Act of 1974, as amended (19
U.S.C. 2273) the Department of Labor
herein presents summaries of
determinations regarding eligibility to
apply for trade adjustment assistance for
workers (TA–W) number and alternative
trade adjustment assistance (ATAA) by
(TA–W) number issued during the
period of January 7 through January 11,
2008.
In order for an affirmative
determination to be made for workers of
a primary firm and a certification issued
regarding eligibility to apply for worker
adjustment assistance, each of the group
eligibility requirements of Section
222(a) of the Act must be met.
I. Section (a)(2)(A) all of the following
must be satisfied:
A. A significant number or proportion
of the workers in such workers’ firm, or
an appropriate subdivision of the firm,
have become totally or partially
separated, or are threatened to become
totally or partially separated;
B. The sales or production, or both, of
such firm or subdivision have decreased
absolutely; and
C. Increased imports of articles like or
directly competitive with articles
produced by such firm or subdivision
have contributed importantly to such
workers’ separation or threat of
separation and to the decline in sales or
production of such firm or subdivision;
or
II. Section (a)(2)(B) both of the
following must be satisfied:
A. A significant number or proportion
of the workers in such workers’ firm, or
an appropriate subdivision of the firm,
have become totally or partially
separated, or are threatened to become
totally or partially separated;
B. There has been a shift in
production by such workers’ firm or
subdivision to a foreign country of
articles like or directly competitive with
articles which are produced by such
firm or subdivision; and
E:\FR\FM\25JAN1.SGM
25JAN1
Agencies
[Federal Register Volume 73, Number 17 (Friday, January 25, 2008)]
[Notices]
[Pages 4630-4633]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E8-1241]
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DEPARTMENT OF JUSTICE
Drug Enforcement Administration
Nasim F. Khan, M.D.; Denial of Application
On June 8, 2007, the Deputy Assistant Administrator, Office of
Diversion Control, Drug Enforcement Administration, issued an Order to
Show Cause to Nasim F. Khan, M.D. (Respondent), of Houston, Texas. The
Show Cause Order proposed the denial of Respondent's pending
application for a DEA Certificate of Registration as a practitioner on
two grounds: (1) That she lacked authority under state law to handle
controlled substances, and (2) that her ``registration would be
inconsistent with the public interest.'' Show Cause Order at 1; see
also 21 U.S.C. 823(f).
The Show Cause Order specifically alleged that ``[o]n June 26,
2006, [Respondent's] Texas Controlled Substance Registration was
terminated,'' and that she was therefore ``not currently authorized by
the State of Texas to prescribe, dispense, or otherwise handle
controlled substances.'' Show Cause Order at 1. The Show Cause Order
further alleged that Respondent had committed acts inconsistent with
the public interest because she had ``allowed [her] DEA registration to
be used to dispense controlled substances for other than legitimate
medical purposes'' and had ``engage[ed] in self-prescribing of
controlled substances, in violation of the Texas Controlled Substances
Act.'' Id.
On June 15, 2007, the Show Cause Order, which also notified
Respondent of her right to request a hearing on the allegations, was
served on Respondent by Federal Express delivered to her residence.
Because: (1) More than thirty days have passed since service of the
Show Cause Order, and (2) neither Respondent, nor anyone purporting to
represent her, has requested a hearing, I conclude that Respondent has
waived her right to a hearing. See 21 CFR 1301.43(d). I therefore enter
this Final Order without a hearing based on relevant material contained
in the
[[Page 4631]]
investigative file, see id. 1301.43(e), and make the following
findings.
Findings
Respondent is a physician with a specialty in psychiatry and
pathology. Respondent previously held a DEA Certificate of Registration
as a practitioner at the registered location of Houston Medical Clinic,
10881 Richmond Ave., Apt. 412, Houston, Texas. In July 2004, DEA
Diversion Investigators with the Houston Field Division received
information that Respondent was prescribing promethazine with codeine
cough syrup, a schedule V controlled substance, see 21 CRR 1308.15(c),
to an individual who had been arrested three times by the Houston
Police Department for unlawfully possessing controlled substances.
In August 2005, DEA Diversion Investigators (DIs) received
information that two unlicensed individuals (F.K. and V.V.), who worked
at the Main Medical Clinic (which was located in Jacinto City, Texas),
were using Respondent's DEA registration to issue controlled-substance
prescriptions for drugs which included Lorcet 10/650 (a branded drug
combining hydrocodone and acetaminophen and a schedule III controlled
substance, see 21 CFR 1308.13(e), Xanax (alprazolam), a schedule IV
controlled substance, see id. 1308.14(c), and promethazine with codeine
cough syrup. Id. 1308.15(c). F.K. and V.V. charged $100 for each
prescription.
The DIs subsequently went to the clinic and interviewed several
people. While the DIs were told that Respondent had terminated her
employment at the clinic, they also obtained a stack of prescription
carbons. The copies indicated the patient's name, the name of a
controlled substance, and Respondent's DEA number. During other
interviews, the DIs determined that Respondent had seen only one or two
``patients'' each day, and that most of the clinic's ``patients'' were
seen by other people including several foreign graduate students who
were not licensed in any field of medical practice. The DIs also
confirmed that V.V. had sold a stack of prescriptions, which bore a
signature similar to Respondent's, for a large amount of cash.
Thereafter, on August 11, 2005, the DIs interviewed Respondent at
the location of a clinic (named the ``45 Clinic'') which she was
opening in Houston and for which she needed to change the address of
her registered location.\1\ During the interview, Respondent stated
that she had seen approximately forty patients a day at the Main
Medical Clinic and that the cost for a controlled-substance
prescription was $80 cash. Respondent further stated that at the
clinic, foreign graduate students worked under her supervision and
wrote the prescriptions which she then signed. Respondent also stated
that she had taken a continuing medical education class in pain
management and that the only controlled substances she prescribed were
Vicodin, Lorcet, and Lortab.\2\
---------------------------------------------------------------------------
\1\ According to the investigative file, Respondent did not own
the clinic.
\2\ Respondent also stated that she prescribed Ritalin for her
child psychiatric patients who had Attention Deficit Disorder.
---------------------------------------------------------------------------
In the course of the investigation, the DIs had previously
determined that Respondent had obtained controlled substances based on
117 prescriptions issued to her under her DEA number. During the
interview, Respondent denied that she had self-prescribed and claimed
that her son was also a physician and had prescribed the controlled
substances for her. Subsequently, the DIs searched the Texas Medical
Board's website and found that there was no listing for her son.
The DIs had also previously determined that between January 1,
2004, and August 11, 2005, Respondent had obtained approximately 474
twenty-five ml. bottles of schedule V cough medicines. When asked as to
why she had ordered the drugs, Respondent maintained that they were
small containers of cough syrup which she used when she was unable to
sleep.
While at Respondent's new clinic, the DIs interviewed V.V., the
same individual who had been implicated in selling controlled-substance
prescriptions at Respondent's former employer. V.V. told the
investigators that she had first met Respondent on that very day (when
she had purportedly interviewed for a position at the clinic) and that
her duties at Respondent's clinic would include scheduling
appointments, taking vital signs, and other duties performed by
receptionists.
Thereafter, on August 30, 2005, a registration technician changed
Respondent's registered location to the address of her new clinic.
Approximately three weeks later, on September 19, 2005, Respondent
notified a DI that V.V. was using her DEA number to write unauthorized
prescriptions for unknown individuals.
Later that day, two DIs interviewed Respondent at her residence.
Respondent told the DIs that she had terminated her employment at the
Main Medical Clinic because she suspected that its owner was involved
in illegal activities. Respondent stated that she had contacted DEA
because she had received information that the Corpus Christi, Texas
Police Department was looking for her regarding prescriptions she had
written. Respondent further stated that during the previous week, she
had gone to her new clinic and attempted to retrieve her prescriptions
but was told that the pads belonged to the clinic. Respondent added
that she had become concerned that someone was using her DEA number to
issue prescriptions without her consent. Because of the unauthorized
use of her number, Respondent then agreed to voluntarily surrender her
DEA registration. She also surrendered her state controlled-substances
registration.
On September 30, 2005, Respondent applied for a new registration
using the address of the 45 Clinic for her proposed registered
location. Several days later, two DIs went to Respondent's residence
and attempted to interview her. Upon opening the door, Respondent
started screaming at the DIs and stated that they should contact her
attorney. When one of the DIs asked Respondent for her attorney's phone
number, Respondent stated that she would get the number and slammed the
door. Several minutes later, Respondent opened the door, threw a piece
of paper at the DI, and stated in a loud voice that ``the White House
knew who her father was and that she was his daughter.'' After the DIs
told Respondent that they were there to speak to her about her
application, Respondent stated that ``there would be no trick or
treating here today.'' One of the DIs again asked Respondent whether
she had applied for a new registration. Respondent answered ``yes'' and
again slammed the door shut.
Thereafter, a local pharmacist notified DEA investigators that on
October 3 and 4, he had received two prescriptions which were written
under Respondent's DEA number. The pharmacist told the DIs that when he
had attempted to verify one the prescriptions, Respondent did not
return the call. Respondent, in a subsequent interview, denied issuing
the prescriptions.
On January 5, 2006, a detective with the Garland, Texas Police
Department notified one of the DIs that numerous prescriptions written
under Respondent's former DEA registration had been presented at a
local pharmacy. The prescriptions bore the name and address of the Main
Medical Clinic, Respondent's former employer.
[[Page 4632]]
Thereafter, on March 28, 2006, an official of the Texas Department
of Public Safety (DPS) notified a DI that the State intended to
terminate Respondent's state controlled-substances registration. The
state official further told the DI that Respondent's application had
been erroneously granted because at the time the application was
approved, the State was upgrading its computer system and was unable to
access her history.
Subsequently, on June 26, 2006, DPS terminated Respondent's state
controlled-substances registration on the ground that she was
prohibited under the State's rules for re-applying for a period of one
year following her surrendering of her state registration. I further
find that the State has not re-instated her controlled-substances
registration.
I also find that on August 24, 2007, Respondent entered into an
Agreed Order with the Texas Medical Board. Under the order, Respondent
voluntarily and permanently surrendered her medical license. According
to the Texas Medical Board's website, ``[t]he action was based on
[Respondent's] failure to meet the standard of care due [to] her non-
therapeutic prescription of controlled substances to four patients and
to herself.''
Discussion
Section 303(f) of the Controlled Substances Act provides that
``[t]he Attorney General shall register practitioners * * * to dispense
* * * controlled substances in schedule II, III, IV, or V, if the
applicant is authorized to dispense * * * controlled substances under
the laws of the State in which he practices.'' 21 U.S.C. 823(f).
Section 303(f) further provides that ``[t]he Attorney General may deny
an application for such registration if he determines that the issuance
of such registration would be inconsistent with the public interest.''
Id. In making the public interest determination, the Act requires the
consideration of the following factors:
(1) The recommendation of the appropriate State licensing board
or professional disciplinary authority.
(2) The applicant's experience in dispensing * * * controlled
substances.
(3) The applicant's conviction record under Federal or State
laws relating to the manufacture, distribution, or dispensing of
controlled substances.
(4) Compliance with applicable State, Federal, or local laws
relating to controlled substances.
(5) Such other conduct which may threaten the public health and
safety.
Id.
``[T]hese factors are * * * considered in the disjunctive.'' Robert
A. Leslie, M.D., 68 FR 15227, 15230 (2003). I ``may rely on any one or
a combination of factors, and may give each factor the weight [I]
deem[] appropriate in determining whether a registration should be
revoked.'' Id. Moreover, I am ``not required to make findings as to all
of the factors.'' Hoxie v. DEA, 419 F.3d 477, 482 (6th Cir. 2005); see
also Morall v. DEA, 412 F.3d 165, 173-74 (DC Cir. 2005).
In this case, I conclude that there are two independent grounds for
denying Respondent's application. First, Respondent is not currently
authorized under Texas law to handle controlled substances and thus
does not meet an essential requirement for a registration under the
CSA. Second, while it appears that Respondent will not be returning to
medical practice anytime soon, her experience in dispensing controlled
substances and her record of compliance with applicable laws make clear
that granting her a registration ``would be inconsistent with the
public interest.'' 21 U.S.C. 823(f).
Under the Controlled Substances Act (CSA), a practitioner must be
currently authorized to handle controlled substances in ``the
jurisdiction in which [she] practices'' in order to maintain a DEA
registration. See 21 U.S.C. 802(21) (``[t]he term `practitioner' means
a physician * * * licensed, registered, or otherwise permitted, by * *
* the jurisdiction in which he practices * * * to distribute, dispense,
[or] administer * * * a controlled substance in the course of
professional practice''). See also id. section 823(f) (``The Attorney
General shall register practitioners * * * if the applicant is
authorized to dispense * * * controlled substances under the laws of
the State in which he practices.''). Relatedly, DEA has repeatedly held
that the CSA requires the revocation of a registration issued to a
practitioner who no longer possesses authority under state law to
handle controlled substances. See Sheran Arden Yeates, 71 FR 39130,
39131 (2006); Dominick A. Ricci, 58 FR 51104, 51105 (1993); Bobby
Watts, 53 FR 11919, 11920 (1988). See also 21 U.S.C. 824(a)(3)
(authorizing the revocation of a registration ``upon a finding that the
registrant * * * has had his State license or registration suspended
[or] revoked * * * and is no longer authorized by State law to engage
in the * * * distribution [or] dispensing of controlled substances'').
Here, the investigative file establishes that Respondent's Texas
controlled-substances registration was terminated on June 26, 2006.
Moreover, there is no evidence that the State has issued a new
controlled substance registration to her, and the Agreed Order which
Respondent entered into with the Texas Medical Board suggests that the
State will not grant her a new controlled-substances registration any
time soon. Because Respondent is without authority to handle controlled
substances in Texas, the State in which she seeks a DEA registration,
she does not meet an essential prerequisite for a new DEA registration.
Accordingly, her application is denied on that basis. See 21 U.S.C.
823(f).
I further note that even if Respondent possessed a state
registration, the record would still support the denial of her
application on the ground that her registration would be ``inconsistent
with the public interest.'' 21 U.S.C. 823(f). As the State found,
Respondent has engaged in the non-therapeutic prescription of
controlled substances both to herself and others.
With respect to her self-prescribing, the record establishes that
Respondent issued to herself 117 prescriptions for narcotic-cough
syrups, which are schedule V controlled substances. The record further
establishes that Respondent's statements to investigators that the
prescriptions were issued to her by her son, and that her son was a
physician, were false.
Moreover, there is also substantial and disturbing evidence that
Respondent failed to exercise proper control over her prescriptions
pads and allowed unlicensed and un-registered individuals at the Main
Medical Clinic to write prescriptions under her DEA registration. This
conduct violates federal law and regulations, which require that a
prescription be ``issued for a legitimate medical purpose by an
individual practitioner acting in the usual course of [her]
professional practice,'' 21 CFR 1306.04(a), and that each person
writing a prescription be ``[a]uthorized to prescribe controlled
substances by the jurisdiction in which he is licensed to practice his
profession and * * * [e]ither registered or exempted from
registration.'' Id. Sec. 1306.03(a). Accordingly, even if Respondent
held a state registration, her abysmal experience in dispensing
controlled substances and her record of non-compliance with federal and
state laws related to controlled substances would nonetheless require
the denial of her application.
Order
Pursuant to the authority vested in me by 21 U.S.C. 823(f), as well
as 28 CFR 0.100(b) & 0.104, I order that the application of Nasim F.
Khan, M.D., for
[[Page 4633]]
a DEA Certificate of Registration as a practitioner be, and it hereby
is, denied. This order is effective February 25, 2008.
Dated: January 17, 2008.
Michele M. Leonhart,
Deputy Administrator.
[FR Doc. E8-1241 Filed 1-24-08; 8:45 am]
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