Matt M. Ahmadi, D.P.M.; Decision and Order, 59454-59455 [2022-21269]
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59454
Federal Register / Vol. 87, No. 189 / Friday, September 30, 2022 / Notices
jspears on DSK121TN23PROD with NOTICES
regarding the estimated public burden
or associated response time,
suggestions, or need a copy of the
proposed information collection
instrument with instructions, or
additional information, please contact:
Shawn C. Stevens, Industry Liaison,
Firearms & Explosives Services
Division, either by mail at 244 Needy
Road Martinsburg, WV 24505, by email
at shawn.stevens@atf.gov, or by
telephone at 304–616–4421.
SUPPLEMENTARY INFORMATION: Written
comments and suggestions from the
public and affected agencies concerning
the proposed collection of information
are encouraged. Your comments should
address one or more of the following
four points:
• 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;
• Evaluate whether and if so how the
quality, utility, and clarity of the
information to be collected can be
enhanced; 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.
Overview of This Information
Collection
1. Type of Information Collection:
Revision of a currently approved
collection.
2. The Title of the Form/Collection:
FEL Out of Business Records.
3. The agency form number, if any,
and the applicable component of the
Department sponsoring the collection:
Form number (if applicable): None.
Sponsor: Bureau of Alcohol, Tobacco,
Firearms and Explosives, U.S.
Department of Justice.
4. Affected public who will be asked
or required to respond, as well as a brief
abstract:
Primary: Business or other for-profit.
Other (if applicable): Individuals or
households.
Abstract: Per 27 CFR 555.128, when
an explosive materials business or
operation is discontinued, the records
must be delivered to the ATF Out of
Business Records Center within 30 days
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18:52 Sep 29, 2022
Jkt 256001
of the business or operations
discontinuance.
5. An estimate of the total number of
respondents and the amount of time
estimated for an average respondent to
respond: An estimated 538 respondents
will utilize this information collection,
and it will take each respondent
approximately 30 minutes to complete
their responses.
6. An estimate of the total public
burden (in hours) associated with the
collection: The estimated annual public
burden associated with this collection is
269 hours, which is equal to 538 (# of
respondents) * 1 (# of responses per
respondents) * .5 (30 minutes).
7. An Explanation of the Change in
Estimates: The adjustments associated
with this information collection include
an increase in the total respondents by
289 respectively, since the last renewal
in 2019. Consequently, the cost burden
has also risen by $70,548 since 2019.
If additional information is required
contact: Robert Houser, Department
Clearance Officer, Policy and Planning
Staff, Office of the Chief Information
Officer, Justice Management Division,
United States Department of Justice,
Two Constitution Square, 145 N Street
NE, 3.E–206, Washington, DC 20530.
Dated: September 27, 2022.
Robert Houser,
Department Clearance Officer, Policy and
Planning Staff, Office of the Chief Information
Officer, U.S. Department of Justice.
[FR Doc. 2022–21292 Filed 9–29–22; 8:45 am]
BILLING CODE 4410–FY–P
DEPARTMENT OF JUSTICE
Drug Enforcement Administration
Matt M. Ahmadi, D.P.M.; Decision and
Order
On February 17, 2022, the Drug
Enforcement Administration
(hereinafter, DEA or Government)
issued an Order to Show Cause
(hereinafter, OSC) to Matt M. Ahmadi,
D.P.M. (hereinafter, Registrant). Request
for Final Agency Action (hereinafter,
RFAA), Exhibit (hereinafter, RFAAX) 2
(OSC), at 1; RFAA, at 1. The OSC
proposed the revocation of Registrant’s
Certificate of Registration No.
BA8767646 at the registered address of
26800 Crown Valley Pkwy, Suite 320,
Mission Viejo, CA 92691. RFAAX 2, at
1. The OSC alleged that Registrant’s
registration should be revoked because
Registrant is ‘‘without authority to
prescribe controlled substances in the
State of California, the state in which
PO 00000
Frm 00066
Fmt 4703
Sfmt 4703
[he is] registered with the DEA.’’ Id. at
2 (citing 21 U.S.C. 824(a)(3)).1
The Agency makes the following
findings of fact based on the
uncontroverted evidence submitted by
the Government in its RFAA,2 which
was submitted on September 6, 2022.3
Findings of Fact
Following an Accusation against
Registrant from the State of California,
Department of Consumer Affairs, Board
of Podiatric Medicine (hereinafter, the
Board), dated May 7, 2019, on March 27,
2020, an Administrative Law Judge from
the State of California, Office of
Administrative Hearings, issued a
Proposed Decision revoking Registrant’s
podiatric medicine license. RFAAX 3,
appendix A, at 3, 38, 39. On June 16,
2020, the Board issued a Decision and
Order accepting and adopting the
Proposed Decision, effective July 16,
2020. Id. at 1.
According to California’s online
records, of which the Agency takes
official notice, Registrant’s license is
still revoked.4 Medical Board of
California License Verification, https://
www.mbc.ca.gov/License-Verification
(last visited date of signature of this
Order). Accordingly, the Agency finds
that Registrant is not licensed to engage
in the practice of medicine in California,
1 According to Agency records, Registrant’s
Certificate of Registration No. BA8767646 expired
on June 30, 2022. The fact that a Registrant allows
his registration to expire during the pendency of an
OSC does not impact the Agency’s jurisdiction or
prerogative under the Controlled Substances Act
(hereinafter, CSA) to adjudicate the OSC to finality.
Jeffrey D. Olsen, M.D., 84 FR 68,474 (2019).
2 The Government’s RFAA is dated July 13, 2022.
RFAA, at 5.
3 Based on a Declaration from a DEA Diversion
Investigator, the Agency finds that the
Government’s service of the OSC on Registrant was
adequate. RFAAX 3, at 1–2. Further, based on the
Government’s assertions in its RFAA, the Agency
finds that more than thirty days have passed since
Registrant was served with the OSC and Registrant
has neither requested a hearing nor submitted a
written statement or corrective action plan and
therefore has waived any such rights. RFAA, at 1,
3; see also 21 CFR 1301.43 and 21 U.S.C. 824(c)(2).
4 Under the Administrative Procedure Act, an
agency ‘‘may take official notice of facts at any stage
in a proceeding—even in the final decision.’’
United States Department of Justice, Attorney
General’s Manual on the Administrative Procedure
Act 80 (1947) (Wm. W. Gaunt & Sons, Inc., Reprint
1979). Pursuant to 5 U.S.C. 556(e), ‘‘[w]hen an
agency decision rests on official notice of a material
fact not appearing in the evidence in the record, a
party is entitled, on timely request, to an
opportunity to show the contrary.’’ Accordingly,
Registrant may dispute the Agency’s finding by
filing a properly supported motion for
reconsideration of findings of fact within fifteen
calendar days of the date of this Order. Any such
motion and response shall be filed and served by
email to the other party and to Office of the
Administrator, Drug Enforcement Administration at
dea.addo.attorneys@dea.usdoj.gov.
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Federal Register / Vol. 87, No. 189 / Friday, September 30, 2022 / Notices
the state in which he is registered with
the DEA.
jspears on DSK121TN23PROD with NOTICES
Discussion
Pursuant to 21 U.S.C. 824(a)(3), the
Attorney General is authorized to
suspend or revoke a registration issued
under section 823 of the CSA ‘‘upon a
finding that the registrant . . . has had
his State license or registration
suspended . . . [or] revoked . . . by
competent State authority and is no
longer authorized by State law to engage
in the . . . dispensing of controlled
substances.’’ With respect to a
practitioner, the DEA has also long held
that the possession of authority to
dispense controlled substances under
the laws of the state in which a
practitioner engages in professional
practice is a fundamental condition for
obtaining and maintaining a
practitioner’s registration. See, e.g.,
James L. Hooper, M.D., 76 FR 71371
(2011), pet. for rev. denied, 481 F. App’x
826 (4th Cir. 2012); Frederick Marsh
Blanton, M.D., 43 FR 27616, 27617
(1978).5
According to California statute,
‘‘dispense’’ means ‘‘to deliver a
controlled substance to an ultimate user
or research subject by or pursuant to the
lawful order of a practitioner, including
the prescribing, furnishing, packaging,
labeling, or compounding necessary to
prepare the substance for that delivery.’’
Cal. Health & Safety Code section 11010
(West 2022). Further, a ‘‘practitioner’’
means a person ‘‘licensed, registered, or
otherwise permitted, to distribute,
dispense, conduct research with respect
to, or administer, a controlled substance
in the course of professional practice or
research in this state.’’ Id. at section
11026(c).
Here, the undisputed evidence in the
record is that Registrant lacks authority
5 This rule derives from the text of two provisions
of the CSA. First, Congress defined the term
‘‘practitioner’’ to mean ‘‘a physician . . . or other
person 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.’’ 21 U.S.C. 802(21). Second, in setting the
requirements for obtaining a practitioner’s
registration, Congress directed that ‘‘[t]he Attorney
General shall register practitioners . . . 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). Because Congress has
clearly mandated that a practitioner possess state
authority in order to be deemed a practitioner under
the CSA, the DEA has held repeatedly that
revocation of a practitioner’s registration is the
appropriate sanction whenever he is no longer
authorized to dispense controlled substances under
the laws of the state in which he practices. See, e.g.,
James L. Hooper, 76 FR at 71371–72; Sheran Arden
Yeates, M.D., 71 FR 39130, 39131 (2006); Dominick
A. Ricci, M.D., 58 FR 51104, 51105 (1993); Bobby
Watts, M.D., 53 FR 11919, 11920 (1988); Frederick
Marsh Blanton, 43 FR at 27617.
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18:52 Sep 29, 2022
Jkt 256001
to practice medicine in California. As
discussed above, a physician must be a
licensed practitioner to dispense a
controlled substance in California.
Thus, because Registrant lacks authority
to practice medicine in California and,
therefore, is not authorized to handle
controlled substances in California,
Registrant is not eligible to maintain a
DEA registration. Accordingly, the
Agency will order that Registrant’s DEA
registration be revoked.
Order
Pursuant to 28 CFR 0.100(b) and the
authority vested in me by 21 U.S.C.
824(a), I hereby revoke DEA Certificate
of Registration No. BA8767646 issued to
Matt M. Ahmadi, D.P.M. Further,
pursuant to 28 CFR 0.100(b) and the
authority vested in me by 21 U.S.C.
823(f), I hereby deny any pending
applications of Matt M. Ahmadi, D.P.M.,
to renew or modify this registration, as
well as any other pending application of
Matt M. Ahmadi, D.P.M., for additional
registration in California. This Order is
effective October 31, 2022.
Signing Authority
This document of the Drug
Enforcement Administration was signed
on September 26, 2022, by
Administrator Anne Milgram. That
document with the original signature
and date is maintained by DEA. For
administrative purposes only, and in
compliance with requirements of the
Office of the Federal Register, the
undersigned DEA Federal Register
Liaison Officer has been authorized to
sign and submit the document in
electronic format for publication, as an
official document of DEA. This
administrative process in no way alters
the legal effect of this document upon
publication in the Federal Register.
Heather Achbach,
Federal Register Liaison Officer, Drug
Enforcement Administration.
[FR Doc. 2022–21269 Filed 9–29–22; 8:45 am]
BILLING CODE 4410–09–P
DEPARTMENT OF JUSTICE
Drug Enforcement Administration
Thomas Blair, M.D.; Decision and
Order
On May 25, 2022, the Drug
Enforcement Administration
(hereinafter, DEA or Government)
issued an Order to Show Cause
(hereinafter, OSC) to Thomas Blair, M.D.
(hereinafter, Registrant). Request for
Final Agency Action (hereinafter,
RFAA), Exhibit (hereinafter, RFAAX) D
PO 00000
Frm 00067
Fmt 4703
Sfmt 4703
59455
(OSC), at 1, 3. The OSC proposed the
revocation of Registrant’s Certificate of
Registration No. AB1253880 at the
registered address of 725 W. La Veta
Avenue, Suite 110, Orange, CA 92868.
Id. at 1. The OSC alleged that
Registrant’s registration should be
revoked because Registrant is ‘‘without
authority to prescribe controlled
substances in the State of California, the
state in which [he is] registered with the
DEA.’’ Id. at 2 (citing 21 U.S.C.
824(a)(3)).
The Agency makes the following
findings of fact based on the
uncontroverted evidence offered by the
Government in its RFAA, which was
submitted on September 8, 2022.1
Findings of Fact
On November 2, 2021, an
Administrative Law Judge from the
State of California, Office of
Administrative Hearings, issued a
Decision and Order suspending
Registrant’s California medical license.
RFAAX B, at 2, 35. According to
California’s online records, of which the
Agency takes official notice, Registrant’s
license is still suspended.2 Medical
Board of California License Verification,
https://www.mbc.ca.gov/LicenseVerification (last visited date of
signature of this Order). Accordingly,
the Agency finds that Registrant is not
currently licensed to engage in the
practice of medicine in California, the
state in which he is registered with the
DEA.
Discussion
Pursuant to 21 U.S.C. 824(a)(3), the
Attorney General is authorized to
1 Based on a Declaration from a DEA Diversion
Investigator, the Agency finds that the
Government’s service of the OSC on Registrant was
adequate. RFAA, Declaration 1, at 2. Further, based
on the Government’s assertions in its RFAA, the
Agency finds that more than thirty days have
passed since Registrant was served with the OSC
and Registrant has neither requested a hearing nor
submitted a written statement or corrective action
plan and therefore has waived any such rights.
RFAA, at 1, 3; see also 21 CFR 1301.43 and 21
U.S.C. 824(c)(2).
2 Under the Administrative Procedure Act, an
agency ‘‘may take official notice of facts at any stage
in a proceeding—even in the final decision.’’
United States Department of Justice, Attorney
General’s Manual on the Administrative Procedure
Act 80 (1947) (Wm. W. Gaunt & Sons, Inc., Reprint
1979). Pursuant to 5 U.S.C. 556(e), ‘‘[w]hen an
agency decision rests on official notice of a material
fact not appearing in the evidence in the record, a
party is entitled, on timely request, to an
opportunity to show the contrary.’’ Accordingly,
Registrant may dispute the Agency’s finding by
filing a properly supported motion for
reconsideration of findings of fact within fifteen
calendar days of the date of this Order. Any such
motion and response shall be filed and served by
email to the other party and to Office of the
Administrator, Drug Enforcement Administration at
dea.addo.attorneys@dea.usdoj.gov.
E:\FR\FM\30SEN1.SGM
30SEN1
Agencies
[Federal Register Volume 87, Number 189 (Friday, September 30, 2022)]
[Notices]
[Pages 59454-59455]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2022-21269]
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DEPARTMENT OF JUSTICE
Drug Enforcement Administration
Matt M. Ahmadi, D.P.M.; Decision and Order
On February 17, 2022, the Drug Enforcement Administration
(hereinafter, DEA or Government) issued an Order to Show Cause
(hereinafter, OSC) to Matt M. Ahmadi, D.P.M. (hereinafter, Registrant).
Request for Final Agency Action (hereinafter, RFAA), Exhibit
(hereinafter, RFAAX) 2 (OSC), at 1; RFAA, at 1. The OSC proposed the
revocation of Registrant's Certificate of Registration No. BA8767646 at
the registered address of 26800 Crown Valley Pkwy, Suite 320, Mission
Viejo, CA 92691. RFAAX 2, at 1. The OSC alleged that Registrant's
registration should be revoked because Registrant is ``without
authority to prescribe controlled substances in the State of
California, the state in which [he is] registered with the DEA.'' Id.
at 2 (citing 21 U.S.C. 824(a)(3)).\1\
---------------------------------------------------------------------------
\1\ According to Agency records, Registrant's Certificate of
Registration No. BA8767646 expired on June 30, 2022. The fact that a
Registrant allows his registration to expire during the pendency of
an OSC does not impact the Agency's jurisdiction or prerogative
under the Controlled Substances Act (hereinafter, CSA) to adjudicate
the OSC to finality. Jeffrey D. Olsen, M.D., 84 FR 68,474 (2019).
---------------------------------------------------------------------------
The Agency makes the following findings of fact based on the
uncontroverted evidence submitted by the Government in its RFAA,\2\
which was submitted on September 6, 2022.\3\
---------------------------------------------------------------------------
\2\ The Government's RFAA is dated July 13, 2022. RFAA, at 5.
\3\ Based on a Declaration from a DEA Diversion Investigator,
the Agency finds that the Government's service of the OSC on
Registrant was adequate. RFAAX 3, at 1-2. Further, based on the
Government's assertions in its RFAA, the Agency finds that more than
thirty days have passed since Registrant was served with the OSC and
Registrant has neither requested a hearing nor submitted a written
statement or corrective action plan and therefore has waived any
such rights. RFAA, at 1, 3; see also 21 CFR 1301.43 and 21 U.S.C.
824(c)(2).
---------------------------------------------------------------------------
Findings of Fact
Following an Accusation against Registrant from the State of
California, Department of Consumer Affairs, Board of Podiatric Medicine
(hereinafter, the Board), dated May 7, 2019, on March 27, 2020, an
Administrative Law Judge from the State of California, Office of
Administrative Hearings, issued a Proposed Decision revoking
Registrant's podiatric medicine license. RFAAX 3, appendix A, at 3, 38,
39. On June 16, 2020, the Board issued a Decision and Order accepting
and adopting the Proposed Decision, effective July 16, 2020. Id. at 1.
According to California's online records, of which the Agency takes
official notice, Registrant's license is still revoked.\4\ Medical
Board of California License Verification, https://www.mbc.ca.gov/License-Verification (last visited date of signature of this Order).
Accordingly, the Agency finds that Registrant is not licensed to engage
in the practice of medicine in California,
[[Page 59455]]
the state in which he is registered with the DEA.
---------------------------------------------------------------------------
\4\ Under the Administrative Procedure Act, an agency ``may take
official notice of facts at any stage in a proceeding--even in the
final decision.'' United States Department of Justice, Attorney
General's Manual on the Administrative Procedure Act 80 (1947) (Wm.
W. Gaunt & Sons, Inc., Reprint 1979). Pursuant to 5 U.S.C. 556(e),
``[w]hen an agency decision rests on official notice of a material
fact not appearing in the evidence in the record, a party is
entitled, on timely request, to an opportunity to show the
contrary.'' Accordingly, Registrant may dispute the Agency's finding
by filing a properly supported motion for reconsideration of
findings of fact within fifteen calendar days of the date of this
Order. Any such motion and response shall be filed and served by
email to the other party and to Office of the Administrator, Drug
Enforcement Administration at [email protected].
---------------------------------------------------------------------------
Discussion
Pursuant to 21 U.S.C. 824(a)(3), the Attorney General is authorized
to suspend or revoke a registration issued under section 823 of the CSA
``upon a finding that the registrant . . . has had his State license or
registration suspended . . . [or] revoked . . . by competent State
authority and is no longer authorized by State law to engage in the . .
. dispensing of controlled substances.'' With respect to a
practitioner, the DEA has also long held that the possession of
authority to dispense controlled substances under the laws of the state
in which a practitioner engages in professional practice is a
fundamental condition for obtaining and maintaining a practitioner's
registration. See, e.g., James L. Hooper, M.D., 76 FR 71371 (2011),
pet. for rev. denied, 481 F. App'x 826 (4th Cir. 2012); Frederick Marsh
Blanton, M.D., 43 FR 27616, 27617 (1978).\5\
---------------------------------------------------------------------------
\5\ This rule derives from the text of two provisions of the
CSA. First, Congress defined the term ``practitioner'' to mean ``a
physician . . . or other person 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.'' 21 U.S.C.
802(21). Second, in setting the requirements for obtaining a
practitioner's registration, Congress directed that ``[t]he Attorney
General shall register practitioners . . . 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). Because
Congress has clearly mandated that a practitioner possess state
authority in order to be deemed a practitioner under the CSA, the
DEA has held repeatedly that revocation of a practitioner's
registration is the appropriate sanction whenever he is no longer
authorized to dispense controlled substances under the laws of the
state in which he practices. See, e.g., James L. Hooper, 76 FR at
71371-72; Sheran Arden Yeates, M.D., 71 FR 39130, 39131 (2006);
Dominick A. Ricci, M.D., 58 FR 51104, 51105 (1993); Bobby Watts,
M.D., 53 FR 11919, 11920 (1988); Frederick Marsh Blanton, 43 FR at
27617.
---------------------------------------------------------------------------
According to California statute, ``dispense'' means ``to deliver a
controlled substance to an ultimate user or research subject by or
pursuant to the lawful order of a practitioner, including the
prescribing, furnishing, packaging, labeling, or compounding necessary
to prepare the substance for that delivery.'' Cal. Health & Safety Code
section 11010 (West 2022). Further, a ``practitioner'' means a person
``licensed, registered, or otherwise permitted, to distribute,
dispense, conduct research with respect to, or administer, a controlled
substance in the course of professional practice or research in this
state.'' Id. at section 11026(c).
Here, the undisputed evidence in the record is that Registrant
lacks authority to practice medicine in California. As discussed above,
a physician must be a licensed practitioner to dispense a controlled
substance in California. Thus, because Registrant lacks authority to
practice medicine in California and, therefore, is not authorized to
handle controlled substances in California, Registrant is not eligible
to maintain a DEA registration. Accordingly, the Agency will order that
Registrant's DEA registration be revoked.
Order
Pursuant to 28 CFR 0.100(b) and the authority vested in me by 21
U.S.C. 824(a), I hereby revoke DEA Certificate of Registration No.
BA8767646 issued to Matt M. Ahmadi, D.P.M. Further, pursuant to 28 CFR
0.100(b) and the authority vested in me by 21 U.S.C. 823(f), I hereby
deny any pending applications of Matt M. Ahmadi, D.P.M., to renew or
modify this registration, as well as any other pending application of
Matt M. Ahmadi, D.P.M., for additional registration in California. This
Order is effective October 31, 2022.
Signing Authority
This document of the Drug Enforcement Administration was signed on
September 26, 2022, by Administrator Anne Milgram. That document with
the original signature and date is maintained by DEA. For
administrative purposes only, and in compliance with requirements of
the Office of the Federal Register, the undersigned DEA Federal
Register Liaison Officer has been authorized to sign and submit the
document in electronic format for publication, as an official document
of DEA. This administrative process in no way alters the legal effect
of this document upon publication in the Federal Register.
Heather Achbach,
Federal Register Liaison Officer, Drug Enforcement Administration.
[FR Doc. 2022-21269 Filed 9-29-22; 8:45 am]
BILLING CODE 4410-09-P