Thomas Andr'e Endicott, D.D.S.; Decision and Order, 13892-13894 [2025-05163]
Download as PDF
13892
Federal Register / Vol. 90, No. 58 / Thursday, March 27, 2025 / Notices
Controlled Substance
Schedule
Opium, raw ......................................................................................................................................................................
Opium extracts ................................................................................................................................................................
Opium fluid extract ..........................................................................................................................................................
Opium tincture .................................................................................................................................................................
Opium, powdered ............................................................................................................................................................
Opium, granulated ...........................................................................................................................................................
Levo-alphacetylmethadol .................................................................................................................................................
Opium poppy ...................................................................................................................................................................
Oxymorphone ..................................................................................................................................................................
Noroxymorphone .............................................................................................................................................................
Poppy Straw Concentrate ...............................................................................................................................................
Phenazocine ....................................................................................................................................................................
Thiafentanil ......................................................................................................................................................................
Piminodine .......................................................................................................................................................................
Racemethorphan .............................................................................................................................................................
Racemorphan ..................................................................................................................................................................
Alfentanil ..........................................................................................................................................................................
Remifentanil .....................................................................................................................................................................
Sufentanil .........................................................................................................................................................................
Carfentanil .......................................................................................................................................................................
Tapentadol .......................................................................................................................................................................
Bezitramide ......................................................................................................................................................................
Fentanyl ...........................................................................................................................................................................
Moramide-intermediate ....................................................................................................................................................
9600
9610
9620
9630
9639
9640
9648
9650
9652
9668
9670
9715
9729
9730
9732
9733
9737
9739
9740
9743
9780
9800
9801
9802
II
II
II
II
II
II
II
II
II
II
II
II
II
II
II
II
II
II
II
II
II
II
II
II
The company plans to import the
listed controlled substances for the use
in the manufacture of exempted
certified reference materials. No other
activities for these drug codes are
authorized for this registration.
Approval of permit applications will
occur only when the registrant’s
business activity is consistent with what
is authorized under 21 U.S.C. 952(a)(2).
Authorization will not extend to the
import of Food and Drug
Administration-approved or nonapproved finished dosage forms for
commercial sale.
Controlled substance
Drug
code
Schedule
Marihuana Extract .............
Marihuana .........................
Tetrahydrocannabinols .....
7350
7360
7370
I
I
I
Matthew Strait,
Deputy Assistant Administrator.
[FR Doc. 2025–05282 Filed 3–26–25; 8:45 am]
BILLING CODE P
DEPARTMENT OF JUSTICE
Drug Enforcement Administration
[Docket No. DEA–1521]
Bulk Manufacturer of Controlled
Substances Application: Royal
Emerald Pharmaceuticals
Drug Enforcement
Administration, Justice.
ACTION: Notice of application.
AGENCY:
lotter on DSK11XQN23PROD with NOTICES1
Drug Code
Royal Emerald
Pharmaceuticals has applied to be
registered as a bulk manufacturer of
basic class(es) of controlled
substance(s). Refer to SUPPLEMENTARY
INFORMATION listed below for further
drug information.
SUMMARY:
VerDate Sep<11>2014
17:43 Mar 26, 2025
Jkt 265001
Registered bulk manufacturers of
the affected basic class(es), and
applicants, therefore, may submit
electronic comments on or objections to
the issuance of the proposed registration
on or before May 27, 2025. Such persons
may also file a written request for a
hearing on the application on or before
May 27, 2025.
DATES:
The Drug Enforcement
Administration requires that all
comments be submitted electronically
through the Federal eRulemaking Portal,
which provides the ability to type short
comments directly into the comment
field on the web page or attach a file for
lengthier comments. Please go to
https://www.regulations.gov and follow
the online instructions at that site for
submitting comments. Upon submission
of your comment, you will receive a
Comment Tracking Number. Please be
aware that submitted comments are not
instantaneously available for public
view on https://www.regulations.gov. If
you have received a Comment Tracking
Number, your comment has been
successfully submitted and there is no
need to resubmit the same comment.
ADDRESSES:
In
accordance with 21 CFR 1301.33(a), this
is notice that on February 25, 2025,
Royal Emerald Pharmaceuticals, 14011
Palm Drive, Building B, Desert Hot
Springs, California 92240–6845, applied
to be registered as a bulk manufacturer
of the following basic class(es) of
controlled substance(s):
SUPPLEMENTARY INFORMATION:
PO 00000
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Fmt 4703
Sfmt 4703
I
The company plans to bulk
manufacture the listed controlled
substance to provide Marihuana
(Cannabis) as botanical raw material
and/or active pharmaceutical
ingredients (API) to Drug Enforcement
Administration-registered researchers
and manufacturers. No other activities
for these drug codes are authorized for
this registration.
Matthew Strait,
Deputy Assistant Administrator.
[FR Doc. 2025–05279 Filed 3–26–25; 8:45 am]
BILLING CODE P
DEPARTMENT OF JUSTICE
Drug Enforcement Administration
Thomas Andr’e Endicott, D.D.S.;
Decision and Order
On March 26, 2024, the Drug
Enforcement Administration (DEA or
Government) issued an Order to Show
Cause (OSC) to Thomas Andr’e
Endicott, D.D.S., of Salt Lake City, Utah
(Registrant). Request for Final Agency
Action (RFAA), Exhibit (RFAAX) 1, at 1,
3. The OSC proposed the revocation of
Registrant’s Certificate of Registration
No. FE3865029, alleging that
Registrant’s registration should be
revoked because Registrant is ‘‘currently
without authority to handle controlled
E:\FR\FM\27MRN1.SGM
27MRN1
Federal Register / Vol. 90, No. 58 / Thursday, March 27, 2025 / Notices
substances in Utah, the state in which
[he is] registered with DEA.’’ Id. at 2
(citing 21 U.S.C. 824(a)(3)).
The OSC notified Registrant of his
right to file a written request for hearing,
and that if he failed to file such a
request, he would be deemed to have
waived his right to a hearing and be in
default. Id. (citing 21 CFR 1301.43).
Here, Registrant did not request a
hearing. RFAA, at 3.1 ‘‘A default, unless
excused, shall be deemed to constitute
a waiver of the registrant’s/applicant’s
right to a hearing and an admission of
the factual allegations of the [OSC].’’ 21
CFR 1301.43(e).
Further, ‘‘[i]n the event that a
registrant . . . is deemed to be in
default . . . DEA may then file a request
for final agency action with the
Administrator, along with a record to
support its request. In such
circumstances, the Administrator may
enter a default final order pursuant to
[21 CFR] § 1316.67.’’ Id. § 1301.43(f)(1).
Here, the Government has requested
final agency action based on Registrant’s
default pursuant to 21 CFR 1301.43(d),
(e), (f)(1), 1301.46. RFAA, at 1; see also
21 CFR 1316.67.
lotter on DSK11XQN23PROD with NOTICES1
Findings of Fact
The Agency finds that, in light of
Registrant’s default, the factual
allegations in the OSC are admitted.
According to the OSC, on February 22,
2024, both Registrant’s Utah dental
1 Based on the Government’s submissions in its
RFAA dated May 24, 2024, the Agency finds that
service of the OSC on Registrant was adequate. An
included declaration from a DEA Diversion
Investigator (DI) indicates that on March 27, 2024,
the DI attempted to personally serve Registrant at
Registrant’s registered address, but Registrant was
not present and had not been seen at the premises
since November 2023. RFAAX 2, at 2. On March 28,
2024, the DI requested that the Phoenix Field
Division perform additional diligence in locating
and serving Registrant with the OSC, which was
ultimately unsuccessful. Id.; see also RFAAX 3, at
1 (attempt by a second Diversion Investigator to
personally serve Registrant with the OSC at
Registrant’s last known address in Arizona on April
5, 2024). On April 8, 2024, the DI emailed a copy
of the OSC to Registrant’s registered email address,
and the email was not returned as undeliverable.
Id.; see also id., Attachment 1, at 1. On the same
date, the DI also mailed copies of the OSC via USPC
certified mail and USPS First Class mail to
Registrant at his registered address, both of which
were returned back to the DI. RFAAX 2, at 2–3; see
also id., Attachments 2–3. Here, the Agency finds
that Registrant was successfully served the OSC by
email and that the DI’s efforts to serve Registrant by
other means were ‘‘ ‘reasonably calculated, under
all the circumstances, to apprise [Registrant] of the
pendency of the action.’ ’’ Jones v. Flowers, 547 U.S.
220, 226 (2006) (quoting Mullane v. Central
Hanover Bank & Trust Co., 339 U.S. 306, 314
(1950)); see also Mohammed S. Aljanaby, M.D., 82
FR 34,552, 34,552 (2017) (finding that service by
email satisfies due process where the email is not
returned as undeliverable and other methods have
been unsuccessful). Therefore, due process notice
requirements have been satisfied.
VerDate Sep<11>2014
17:43 Mar 26, 2025
Jkt 265001
license and Utah controlled substance
license were revoked. RFAAX 1, at 1–
2. According to Utah online records, of
which the Agency takes official notice,2
both Registrant’s Utah dental license
and Utah controlled substance license
remain revoked. Utah Division of
Professional Licensing License Lookup
& Verification System, https://
secure.utah.gov/llv/search/search.html
(last visited date of signature of this
Order). Accordingly, the Agency finds
that Registrant is not licensed to
practice as a dentist nor to handle
controlled substances in Utah, the state
in which he is registered with DEA.3
Discussion
Pursuant to 21 U.S.C. 824(a)(3), the
Attorney General is authorized to
suspend or revoke a registration issued
under 21 U.S.C. 823 ‘‘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, 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. Gonzales v.
Oregon, 546 U.S. 243, 270 (2006) (‘‘The
Attorney General can register a
physician to dispense controlled
substances ‘if the applicant is
authorized to dispense . . . controlled
substances under the laws of the State
in which he practices.’ . . . The very
definition of a ‘practitioner’ eligible to
prescribe includes physicians ‘licensed,
registered, or otherwise permitted, by
the United States or the jurisdiction in
which he practices’ to dispense
controlled substances. § 802(21).’’). The
Agency has applied these principles
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).
3 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.’’ The material fact here is that
Registrant, as of the date of this decision, is not
licensed to practice as a dentist in Utah.
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 the DEA Office of
the Administrator, Drug Enforcement
Administration at dea.addo.attorneys@dea.gov.
PO 00000
Frm 00042
Fmt 4703
Sfmt 4703
13893
consistently. See, e.g., James L. Hooper,
M.D., 76 FR 71,371, 71,372 (2011), pet.
for rev. denied, 481 F. App’x 826 (4th
Cir. 2012); Frederick Marsh Blanton,
M.D., 43 FR 27,616, 27,617 (1978).4
Under Utah statute, ‘‘[e]very person
who manufactures, produces,
distributes, prescribes, dispenses,
administers, conducts research with, or
performs laboratory analysis upon any
controlled substance in Schedules I
through V within [the] state . . . shall
obtain a license issued by the [Division
of Professional Licensing].’’ Utah Code
Ann. § 58–37–6(2)(a)(i) (2024).
Here, the undisputed evidence in the
record is that Registrant lacks authority
to handle controlled substances in Utah
because both Registrant’s Utah dental
license and Registrant’s Utah controlled
substance license are revoked. As
discussed above, an individual must
hold a Utah controlled substance license
to dispense a controlled substance in
Utah. Thus, because Registrant lacks
authority to handle controlled
substances in Utah, 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. FE3865029 issued to
Thomas Andr’e Endicott, D.D.S.
Further, pursuant to 28 CFR 0.100(b)
and the authority vested in me by 21
U.S.C. 823(g)(1), I hereby deny any
pending applications of Thomas Andr’e
Endicott, D.D.S., to renew or modify this
registration, as well as any other
pending application of Thomas Andr’e
4 This rule derives from the text of two provisions
of the Controlled Substances Act (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(g)(1). Because Congress
has clearly mandated that a practitioner possess
state authority in order to be deemed a practitioner
under the CSA, 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, M.D., 76 FR at 71,371–72; Sheran
Arden Yeates, M.D., 71 FR 39,130, 39,131 (2006);
Dominick A. Ricci, M.D., 58 FR 51,104, 51,105
(1993); Bobby Watts, M.D., 53 FR 11,919, 11,920
(1988); Frederick Marsh Blanton, M.D., 43 FR at
27,617.
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13894
Federal Register / Vol. 90, No. 58 / Thursday, March 27, 2025 / Notices
Endicott, D.D.S., for additional
registration in Utah. This Order is
effective April 28, 2025.
Signing Authority
This document of the Drug
Enforcement Administration was signed
on March 21, 2025, by Acting
Administrator Derek Maltz. 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.
In
accordance with 21 CFR 1301.34(a), this
is notice that on February 17, 2025,
SpecGx LLC, 3600 North 2nd Street,
Saint Louis, Missouri 63147–3457,
applied to be registered as an importer
of the following basic class(es) of
controlled substance(s):
SUPPLEMENTARY INFORMATION:
[FR Doc. 2025–05163 Filed 3–26–25; 8:45 am]
BILLING CODE 4410–09–P
DEPARTMENT OF JUSTICE
Drug Enforcement Administration
[Docket No. DEA1516]
Controlled substance
Importer of Controlled Substances
Application: SpecGx LLC
Drug Enforcement
Administration Justice.
ACTION: Notice of application.
AGENCY:
SpecGx LLC has applied to be
registered as an importer of basic
class(es) of controlled substance(s).
Refer to SUPPLEMENTARY INFORMATION
listed below for further drug
information.
DATES: Registered bulk manufacturers of
the affected basic class(es), and
applicants therefore, may submit
electronic comments on or objections to
the issuance of the proposed registration
on or before April 28, 2025. Such
persons may also file a written request
for a hearing on the application on or
before April 28, 2025.
ADDRESSES: The Drug Enforcement
Administration requires that all
comments be submitted electronically
through the Federal eRulemaking Portal,
which provides provides the ability to
type short comments directly into the
comment field on the web page or attach
a file for lengthier comments. Please go
to https://www.regulations.gov and
follow the online instructions at that
site for submitting comments. Upon
submission of your comment, you will
lotter on DSK11XQN23PROD with NOTICES1
SUMMARY:
VerDate Sep<11>2014
17:43 Mar 26, 2025
receive a Comment Tracking Number.
Please be aware that submitted
comments are not instantaneously
available for public view on https://
www.regulations.gov. If you have
received a Comment Tracking Number,
your comment has been successfully
submitted and there is no need to
resubmit the same comment. All
requests for a hearing must be sent to (1)
Drug Enforcement administration, Attn:
Hearing Clerk/OALJ, 8701 Morrissette
Drive, Springfield, Virginia 22152, and
(2) Drug Enforcement Administration,
Attn: DEA Federal Register
Representative/DPW, 8701 Morrissette
Drive, Springfield, Virginia 22152. All
requests for a hearing should also be
sent to: Drug Enforcement
Administration, Attn: Administrator,
8701 Morrissette Drive, Springfield,
Virginia 22152.
Jkt 265001
Phenylacetone .................
Coca Leaves ...................
Thebaine ..........................
Opium, raw ......................
Poppy Straw Concentrate
Tapentadol ......................
Drug
code
Schedule
8501
9040
9333
9600
9670
9780
II
II
II
II
II
II
The company plans to import the
listed controlled substances for bulk
manufacture into Active Pharmaceutical
Ingredients for distribution to its
customers. In reference to Tapentadol
(9780) and Thebaine (9333), the
company plans to import intermediate
forms of these controlled substances for
further manufacturing prior to
distribution to its customers. No other
activities for these drugs are authorized
for this registration. Placement of these
codes onto the company’s registration
does not translate into automatic
approval of subsequent permit
applications to import controlled
substances.
Approval of permit applications will
occur only when the registrant’s
business activity is consistent with what
is authorized under 21 U.S.C. 952(a)(2).
Authorization will not extend to the
import of Food and Dru Administration
PO 00000
Frm 00043
Fmt 4703
Sfmt 4703
approved or non-approved finished
dosage forms for commercial sale.
Matthew Strait,
Deputy Assistant Administrator.
[FR Doc. 2025–05278 Filed 3–26–25; 8:45 am]
BILLING CODE P
OFFICE OF PERSONNEL
MANAGEMENT
Submission for Review: 3206–0206,
Evidence To Prove Dependency of a
Child, RI 25–37
Office of Personnel
Management.
ACTION: 60-Day notice and request for
comments.
AGENCY:
Office of Personnel
Management (OPM) Retirement Services
offers the general public and other
federal agencies the opportunity to
comment on the reinstatement of an
expired information collection request
(ICR), Evidence to Prove Dependency of
a Child, RI 25–37.
DATES: Comments are encouraged and
will be accepted until May 27, 2025.
ADDRESSES: You may submit comments,
identified by docket number and/or
OMB Control Number and title, by the
following method:
—Federal Rulemaking Portal: https://
www.regulations.gov. Follow the
instructions for submitting comments.
All submissions received must
include the agency name and docket
number or RIN for this document. The
general policy for comments and other
submissions from members of the public
is to make these submissions available
for public viewing at https://
www.regulations.gov as they are
received without change, including any
personal identifiers or contact
information.
SUMMARY:
A
copy of this ICR with applicable
supporting documentation may be
obtained by contacting the Retirement
Services Publications Team, Office of
Personnel Management, 1900 E Street
NW, Room 3316–L, Washington, DC
20415, Attention: Cyrus S. Benson, or
sent via electronic mail to
RSPublicationsTeam@opm.gov or faxed
to (202) 606–0910 or via telephone at
(202) 936–0401.
SUPPLEMENTARY INFORMATION: As
required by the Paperwork Reduction
Act of 1995 (Pub. L. 104–13, 44 U.S.C.
chapter 35) as amended by the ClingerCohen Act (Pub. L. 104–106), OPM is
soliciting comments for this collection
(OMB No. 3206–0206).
FOR FURTHER INFORMATION CONTACT:
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27MRN1
Agencies
[Federal Register Volume 90, Number 58 (Thursday, March 27, 2025)]
[Notices]
[Pages 13892-13894]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2025-05163]
-----------------------------------------------------------------------
DEPARTMENT OF JUSTICE
Drug Enforcement Administration
Thomas Andr'e Endicott, D.D.S.; Decision and Order
On March 26, 2024, the Drug Enforcement Administration (DEA or
Government) issued an Order to Show Cause (OSC) to Thomas Andr'e
Endicott, D.D.S., of Salt Lake City, Utah (Registrant). Request for
Final Agency Action (RFAA), Exhibit (RFAAX) 1, at 1, 3. The OSC
proposed the revocation of Registrant's Certificate of Registration No.
FE3865029, alleging that Registrant's registration should be revoked
because Registrant is ``currently without authority to handle
controlled
[[Page 13893]]
substances in Utah, the state in which [he is] registered with DEA.''
Id. at 2 (citing 21 U.S.C. 824(a)(3)).
The OSC notified Registrant of his right to file a written request
for hearing, and that if he failed to file such a request, he would be
deemed to have waived his right to a hearing and be in default. Id.
(citing 21 CFR 1301.43). Here, Registrant did not request a hearing.
RFAA, at 3.\1\ ``A default, unless excused, shall be deemed to
constitute a waiver of the registrant's/applicant's right to a hearing
and an admission of the factual allegations of the [OSC].'' 21 CFR
1301.43(e).
---------------------------------------------------------------------------
\1\ Based on the Government's submissions in its RFAA dated May
24, 2024, the Agency finds that service of the OSC on Registrant was
adequate. An included declaration from a DEA Diversion Investigator
(DI) indicates that on March 27, 2024, the DI attempted to
personally serve Registrant at Registrant's registered address, but
Registrant was not present and had not been seen at the premises
since November 2023. RFAAX 2, at 2. On March 28, 2024, the DI
requested that the Phoenix Field Division perform additional
diligence in locating and serving Registrant with the OSC, which was
ultimately unsuccessful. Id.; see also RFAAX 3, at 1 (attempt by a
second Diversion Investigator to personally serve Registrant with
the OSC at Registrant's last known address in Arizona on April 5,
2024). On April 8, 2024, the DI emailed a copy of the OSC to
Registrant's registered email address, and the email was not
returned as undeliverable. Id.; see also id., Attachment 1, at 1. On
the same date, the DI also mailed copies of the OSC via USPC
certified mail and USPS First Class mail to Registrant at his
registered address, both of which were returned back to the DI.
RFAAX 2, at 2-3; see also id., Attachments 2-3. Here, the Agency
finds that Registrant was successfully served the OSC by email and
that the DI's efforts to serve Registrant by other means were ``
`reasonably calculated, under all the circumstances, to apprise
[Registrant] of the pendency of the action.' '' Jones v. Flowers,
547 U.S. 220, 226 (2006) (quoting Mullane v. Central Hanover Bank &
Trust Co., 339 U.S. 306, 314 (1950)); see also Mohammed S. Aljanaby,
M.D., 82 FR 34,552, 34,552 (2017) (finding that service by email
satisfies due process where the email is not returned as
undeliverable and other methods have been unsuccessful). Therefore,
due process notice requirements have been satisfied.
---------------------------------------------------------------------------
Further, ``[i]n the event that a registrant . . . is deemed to be
in default . . . DEA may then file a request for final agency action
with the Administrator, along with a record to support its request. In
such circumstances, the Administrator may enter a default final order
pursuant to [21 CFR] Sec. 1316.67.'' Id. Sec. 1301.43(f)(1). Here,
the Government has requested final agency action based on Registrant's
default pursuant to 21 CFR 1301.43(d), (e), (f)(1), 1301.46. RFAA, at
1; see also 21 CFR 1316.67.
Findings of Fact
The Agency finds that, in light of Registrant's default, the
factual allegations in the OSC are admitted. According to the OSC, on
February 22, 2024, both Registrant's Utah dental license and Utah
controlled substance license were revoked. RFAAX 1, at 1-2. According
to Utah online records, of which the Agency takes official notice,\2\
both Registrant's Utah dental license and Utah controlled substance
license remain revoked. Utah Division of Professional Licensing License
Lookup & Verification System, https://secure.utah.gov/llv/search/search.html (last visited date of signature of this Order).
Accordingly, the Agency finds that Registrant is not licensed to
practice as a dentist nor to handle controlled substances in Utah, the
state in which he is registered with DEA.\3\
---------------------------------------------------------------------------
\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).
\3\ 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.'' The material fact here is
that Registrant, as of the date of this decision, is not licensed to
practice as a dentist in Utah. 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 the DEA 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 21 U.S.C. 823 ``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, 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.
Gonzales v. Oregon, 546 U.S. 243, 270 (2006) (``The Attorney General
can register a physician to dispense controlled substances `if the
applicant is authorized to dispense . . . controlled substances under
the laws of the State in which he practices.' . . . The very definition
of a `practitioner' eligible to prescribe includes physicians
`licensed, registered, or otherwise permitted, by the United States or
the jurisdiction in which he practices' to dispense controlled
substances. Sec. 802(21).''). The Agency has applied these principles
consistently. See, e.g., James L. Hooper, M.D., 76 FR 71,371, 71,372
(2011), pet. for rev. denied, 481 F. App'x 826 (4th Cir. 2012);
Frederick Marsh Blanton, M.D., 43 FR 27,616, 27,617 (1978).\4\
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\4\ This rule derives from the text of two provisions of the
Controlled Substances Act (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(g)(1). Because Congress has clearly mandated that a
practitioner possess state authority in order to be deemed a
practitioner under the CSA, 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, M.D., 76 FR at 71,371-72; Sheran Arden
Yeates, M.D., 71 FR 39,130, 39,131 (2006); Dominick A. Ricci, M.D.,
58 FR 51,104, 51,105 (1993); Bobby Watts, M.D., 53 FR 11,919, 11,920
(1988); Frederick Marsh Blanton, M.D., 43 FR at 27,617.
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Under Utah statute, ``[e]very person who manufactures, produces,
distributes, prescribes, dispenses, administers, conducts research
with, or performs laboratory analysis upon any controlled substance in
Schedules I through V within [the] state . . . shall obtain a license
issued by the [Division of Professional Licensing].'' Utah Code Ann.
Sec. 58-37-6(2)(a)(i) (2024).
Here, the undisputed evidence in the record is that Registrant
lacks authority to handle controlled substances in Utah because both
Registrant's Utah dental license and Registrant's Utah controlled
substance license are revoked. As discussed above, an individual must
hold a Utah controlled substance license to dispense a controlled
substance in Utah. Thus, because Registrant lacks authority to handle
controlled substances in Utah, 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.
FE3865029 issued to Thomas Andr'e Endicott, D.D.S. Further, pursuant to
28 CFR 0.100(b) and the authority vested in me by 21 U.S.C. 823(g)(1),
I hereby deny any pending applications of Thomas Andr'e Endicott,
D.D.S., to renew or modify this registration, as well as any other
pending application of Thomas Andr'e
[[Page 13894]]
Endicott, D.D.S., for additional registration in Utah. This Order is
effective April 28, 2025.
Signing Authority
This document of the Drug Enforcement Administration was signed on
March 21, 2025, by Acting Administrator Derek Maltz. 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. 2025-05163 Filed 3-26-25; 8:45 am]
BILLING CODE 4410-09-P