Willard J. Davis, D.O.; Decision and Order, 13881-13882 [2025-05166]
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Federal Register / Vol. 90, No. 58 / Thursday, March 27, 2025 / Notices
established a schedule for the final
phase of the antidumping duty
investigations (89 FR 91423, November
19, 2024). On March 19, 2025, counsel
for Eastman Chemical Company
(‘‘Eastman’’) and counsel for BASF
Corporation (‘‘BASF’’) filed requests to
appear at the hearing. No other parties
submitted a request to appear at the
hearing. On March 20, 2025, counsel for
Eastman filed a request that the
Commission cancel the scheduled
hearing for these investigations and
withdrew its request to appear at the
hearing. On March 20, 2025, counsel for
BASF withdrew its request to appear at
the hearing. Counsel indicated a
willingness to respond to any
Commission questions in lieu of an
actual hearing. Consequently, the public
hearing in connection with these
investigations, scheduled to begin at
9:30 a.m. on Tuesday, March 25, 2025,
is cancelled. Parties to these
investigations should respond to any
written questions posed by the
Commission in their posthearing briefs,
which are due to be filed on April 1,
2025.
For further information concerning
these investigations see the
Commission’s notice cited above and
the Commission’s Rules of Practice and
Procedure, part 201, subparts A and B
(19 CFR part 201), and part 207,
subparts A, D, E, and F (19 CFR part
207).
Authority: These investigations are
being conducted under authority of title
VII of the Tariff Act of 1930; this notice
is published pursuant to § 207.21 of the
Commission’s rules.
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 May 27, 2025. Such persons
may also file a written request for a
hearing on the application on or before
May 27, 2025.
ADDRESSES: 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.
SUPPLEMENTARY INFORMATION: In
accordance with 21 CFR 1301.33(a), this
is notice that on February 26, 2025,
Promega Corporation, 3075 Sub Zero
Parkway, Fitchburg, Wisconsin 53719,
applied to be registered as bulk
manufacturer of the following basic
class(es) of controlled substance(s):
By order of the Commission.
Issued: March 24, 2025.
Lisa Barton,
Secretary to the Commission.
Psilocybin ........................
Psilocyn ...........................
[FR Doc. 2025–05271 Filed 3–26–25; 8:45 am]
BILLING CODE 7020–02–P
DEPARTMENT OF JUSTICE
Controlled substance
I
Drug
code
Schedule
7437
7438
I
I
I
The company plans to bulk
manufacture the listed controlled
substances as Active Pharmaceutical
Ingredients (API) for sale to its
customers. No other activities for these
drug codes are authorized for this
registration.
Drug Enforcement Administration
Matthew Strait,
Deputy Assistant Administrator.
[Docket No. DEA–1526]
[FR Doc. 2025–05283 Filed 3–26–25; 8:45 am]
BILLING CODE P
lotter on DSK11XQN23PROD with NOTICES1
Bulk Manufacturer of Controlled
Substances Application; Promega
Corporation
Drug Enforcement
Administration, Justice.
ACTION: Notice of application.
AGENCY:
Promega Corporation has
applied to be registered as a bulk
manufacturer of basic class(es) of
controlled substance(s). Refer to
SUMMARY:
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17:43 Mar 26, 2025
Jkt 265001
DEPARTMENT OF JUSTICE
Drug Enforcement Administration
[Docket No. 25–19]
Willard J. Davis, D.O.; Decision and
Order
On November 13, 2024, the Drug
Enforcement Administration (DEA or
PO 00000
Frm 00030
Fmt 4703
Sfmt 4703
13881
Government) issued an Order to Show
Cause (OSC) to Willard J. Davis, D.O., of
Round Rock, Texas (Respondent). OSC,
at 1, 4. The OSC proposed the
revocation of Respondent’s DEA
Certificate of Registration No.
BD9134254, alleging that Respondent’s
DEA registration should be revoked
because Respondent is ‘‘without
authority to handle controlled
substances in the State of Texas, the
state in which [he is] registered with
DEA.’’ Id. at 2 (citing 21 U.S.C.
824(a)(3)).
On December 10, 2024 Respondent
filed a request for a hearing. On
December 30, 2024, the Government
filed a Motion for Summary Disposition,
which Respondent opposed. On January
23, 2025, Administrative Law Judge
Teresa A. Wallbaum (the ALJ) granted
the Government’s Motion for Summary
Disposition and recommended the
revocation of Respondent’s registration,
finding that because Respondent lacks
state authority to handle controlled
substances in Texas, the state in which
he is registered with DEA, ‘‘[t]here is no
genuine issue of material fact in this
case.’’ Order Granting the Government’s
Motion for Summary Disposition, and
Recommended Rulings, Findings of
Fact, Conclusions of Law, and Decision
of the Administrative Law Judge (RD), at
6. Respondent did not file exceptions to
the RD.
Having reviewed the entire record, the
Agency adopts and hereby incorporates
by reference the entirety of the ALJ’s
rulings, findings of fact, conclusions of
law, and recommended sanction as
found in the RD and summarizes and
expands upon portions thereof herein.
Findings of Fact
On May 16, 2024, the Texas Medical
Board suspended Respondent’s Texas
medical license. RD, at 3.1 According to
Texas online records, of which the
Agency takes official notice,
Respondent’s Texas medical license
remains suspended.2 Texas Medical
Board Healthcare Provider Search,
https://profile.tmb.state.tx.us (last
visited date of signature of this Order).
Accordingly, the Agency finds that
Respondent is not currently licensed to
1 See also Government’s Notice of Filing of
Evidence and Motion for Summary Disposition,
Exhibit 1, at 3–6.
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).
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27MRN1
13882
Federal Register / Vol. 90, No. 58 / Thursday, March 27, 2025 / Notices
practice medicine in Texas, the state in
which he is registered with DEA.3
lotter on DSK11XQN23PROD with NOTICES1
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 Controlled
Substances Act (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, 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
consistently. See, e.g., James L. Hooper,
M.D., 76 FR 71371, 71372 (2011), pet.
for rev. denied, 481 F. App’x 826 (4th
Cir. 2012); Frederick Marsh Blanton,
M.D., 43 FR 27616, 27617 (1978).4
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 medicine in Texas.
Accordingly, Respondent 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.gov.
4 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(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
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17:43 Mar 26, 2025
Jkt 265001
According to Texas statute,
‘‘dispense’’ means ‘‘the delivery of a
controlled substance in the course of
professional practice or research, by a
practitioner or person acting under the
lawful order of a practitioner, to an
ultimate user or research subject. The
term includes the prescribing,
administering, packaging, labeling, or
compounding necessary to prepare the
substance for delivery.’’ Tex. Health &
Safety Code Ann. section 481.002(12)
(2024). Further, a ‘‘practitioner’’
includes ‘‘a physician . . . or other
person licensed, registered, or otherwise
permitted to distribute, dispense,
analyze, conduct research with respect
to, or administer a controlled substance
in the course of professional practice or
research in this state.’’ Id.
section 481.002(39)(A).
Here, the undisputed evidence in the
record is that Respondent lacks
authority to practice medicine in Texas.
As discussed above, an individual must
be a licensed practitioner to dispense a
controlled substance in Texas. Thus,
because Respondent lacks authority to
practice medicine in Texas and,
therefore, is not authorized to handle
controlled substances in Texas,
Respondent is not eligible to maintain a
DEA registration. RD, at 6. Accordingly,
the Agency will order that Respondent’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. BD9134254 issued to
Willard J. Davis, D.O. 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 Willard J. Davis, D.O., to renew or
modify this registration, as well as any
other pending application of Willard J.
Davis, D.O., for additional registration
in Texas. This Order is effective April
28, 2025.
Signing Authority
This document of the Drug
Enforcement Administration was signed
on March 20, 2025, by Acting
Administrator Derek Maltz. That
document with the original signature
and date is maintained by DEA. For
administrative purposes only, and in
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 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, M.D., 43 FR
27617.
PO 00000
Frm 00031
Fmt 4703
Sfmt 4703
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. 2025–05166 Filed 3–26–25; 8:45 am]
BILLING CODE 4410–09–P
DEPARTMENT OF JUSTICE
Drug Enforcement Administration
[Docket No. 25–9]
Joely Keen, A.P.R.N.; Decision and
Order
On September 24, 2024, the Drug
Enforcement Administration (DEA or
Government) issued an Order to Show
Cause (OSC) to Joely Keen, A.P.R.N., of
The Woodlands, Texas (Respondent).
OSC, at 1, 4. The OSC proposed the
revocation of Respondent’s DEA
Certificate of Registration No.
MK4402210, alleging that Respondent’s
DEA registration should be revoked
because Respondent is ‘‘without
authority to prescribe, administer,
dispense, or otherwise handle
controlled substances in the State of
Texas, the state in which [she is]
registered with DEA.’’ Id. at 2 (citing 21
U.S.C. 824(a)(3)).
On October 22, 2024, Respondent
requested a hearing,1 and on October 23,
2024, Respondent filed an Answer to
the allegations in the OSC. See Order
For Respondent To File Answer. On
November 1, 2024, the Government filed
a Motion for Summary Disposition, to
which Respondent did not respond. On
November 19, 2024, Administrative Law
Judge Paul E. Soeffing (the ALJ) granted
the Government’s Motion for Summary
Disposition and recommended the
revocation of Respondent’s registration,
finding that because Respondent lacks
state authority to handle controlled
substances in Texas, the state in which
1 Respondent initially responded to the OSC via
email on October 18, 2024, but her email did not
include a hearing request. See Respondent’s
Request for Hearing (October 18, 2024). On October
21, 2024, the Administrative Law Judge (ALJ)
directed Respondent to file a request for a hearing
if she desired one, along with an answer to the
allegations in the OSC. Order for Respondent to File
Request for Hearing and Answer and for
Government to File Evidence of Lack of State
Authority.
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Agencies
[Federal Register Volume 90, Number 58 (Thursday, March 27, 2025)]
[Notices]
[Pages 13881-13882]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2025-05166]
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DEPARTMENT OF JUSTICE
Drug Enforcement Administration
[Docket No. 25-19]
Willard J. Davis, D.O.; Decision and Order
On November 13, 2024, the Drug Enforcement Administration (DEA or
Government) issued an Order to Show Cause (OSC) to Willard J. Davis,
D.O., of Round Rock, Texas (Respondent). OSC, at 1, 4. The OSC proposed
the revocation of Respondent's DEA Certificate of Registration No.
BD9134254, alleging that Respondent's DEA registration should be
revoked because Respondent is ``without authority to handle controlled
substances in the State of Texas, the state in which [he is] registered
with DEA.'' Id. at 2 (citing 21 U.S.C. 824(a)(3)).
On December 10, 2024 Respondent filed a request for a hearing. On
December 30, 2024, the Government filed a Motion for Summary
Disposition, which Respondent opposed. On January 23, 2025,
Administrative Law Judge Teresa A. Wallbaum (the ALJ) granted the
Government's Motion for Summary Disposition and recommended the
revocation of Respondent's registration, finding that because
Respondent lacks state authority to handle controlled substances in
Texas, the state in which he is registered with DEA, ``[t]here is no
genuine issue of material fact in this case.'' Order Granting the
Government's Motion for Summary Disposition, and Recommended Rulings,
Findings of Fact, Conclusions of Law, and Decision of the
Administrative Law Judge (RD), at 6. Respondent did not file exceptions
to the RD.
Having reviewed the entire record, the Agency adopts and hereby
incorporates by reference the entirety of the ALJ's rulings, findings
of fact, conclusions of law, and recommended sanction as found in the
RD and summarizes and expands upon portions thereof herein.
Findings of Fact
On May 16, 2024, the Texas Medical Board suspended Respondent's
Texas medical license. RD, at 3.\1\ According to Texas online records,
of which the Agency takes official notice, Respondent's Texas medical
license remains suspended.\2\ Texas Medical Board Healthcare Provider
Search, https://profile.tmb.state.tx.us (last visited date of signature
of this Order).
---------------------------------------------------------------------------
\1\ See also Government's Notice of Filing of Evidence and
Motion for Summary Disposition, Exhibit 1, at 3-6.
\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).
---------------------------------------------------------------------------
Accordingly, the Agency finds that Respondent is not currently
licensed to
[[Page 13882]]
practice medicine in Texas, the state in which he is registered with
DEA.\3\
---------------------------------------------------------------------------
\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 medicine in Texas. Accordingly, Respondent 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
Controlled Substances Act (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, 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 71371, 71372 (2011), pet. for rev. denied, 481 F.
App'x 826 (4th Cir. 2012); Frederick Marsh Blanton, M.D., 43 FR 27616,
27617 (1978).\4\
---------------------------------------------------------------------------
\4\ 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(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 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, M.D., 43 FR 27617.
---------------------------------------------------------------------------
According to Texas statute, ``dispense'' means ``the delivery of a
controlled substance in the course of professional practice or
research, by a practitioner or person acting under the lawful order of
a practitioner, to an ultimate user or research subject. The term
includes the prescribing, administering, packaging, labeling, or
compounding necessary to prepare the substance for delivery.'' Tex.
Health & Safety Code Ann. section 481.002(12) (2024). Further, a
``practitioner'' includes ``a physician . . . or other person licensed,
registered, or otherwise permitted to distribute, dispense, analyze,
conduct research with respect to, or administer a controlled substance
in the course of professional practice or research in this state.'' Id.
section 481.002(39)(A).
Here, the undisputed evidence in the record is that Respondent
lacks authority to practice medicine in Texas. As discussed above, an
individual must be a licensed practitioner to dispense a controlled
substance in Texas. Thus, because Respondent lacks authority to
practice medicine in Texas and, therefore, is not authorized to handle
controlled substances in Texas, Respondent is not eligible to maintain
a DEA registration. RD, at 6. Accordingly, the Agency will order that
Respondent'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.
BD9134254 issued to Willard J. Davis, D.O. 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 Willard J. Davis, D.O., to
renew or modify this registration, as well as any other pending
application of Willard J. Davis, D.O., for additional registration in
Texas. This Order is effective April 28, 2025.
Signing Authority
This document of the Drug Enforcement Administration was signed on
March 20, 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. 2025-05166 Filed 3-26-25; 8:45 am]
BILLING CODE 4410-09-P