Darryl L. Henry, M.D.; Decision and Order, 54479-54480 [2021-21425]
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Federal Register / Vol. 86, No. 188 / Friday, October 1, 2021 / Notices
Stat. Ann. § 30–31–12(A) (West, current
through the end of the First Regular
Session and First Special Session, 55th
Legislature (2021)). In turn, ‘‘dispense’’
means ‘‘to deliver a controlled
substance to an ultimate user or
research subject pursuant to the lawful
order of a practitioner, including the
administering, prescribing, packaging,
labeling or compounding necessary to
prepare the controlled substance for that
delivery.’’ Id. at § 30–31–2(H). Further,
a ‘‘practitioner’’ means ‘‘a physician
. . . dentist . . . or other person
licensed or certified to prescribe and
administer drugs that are subject to the
Controlled Substances Act.’’ Id. at § 30–
31–2(P).
Here, the undisputed evidence in the
record is that Respondent’s New Mexico
controlled substance license is expired;
therefore, he cannot dispense controlled
substances in New Mexico. Further,
Respondent’s New Mexico dental
license has been revoked. As such, he is
not a ‘‘practitioner’’ licensed or certified
to prescribe and administer a controlled
substance under New Mexico law. Thus,
because Respondent lacks authority to
handle controlled substances in New
Mexico, Respondent is not eligible to
maintain a DEA registration.
Accordingly, I 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. BG9826427 issued to
William C. Gardner, D.D.S. 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
application of William C. Gardner to
renew or modify this registration, as
well as any other pending application of
William C. Gardner, D.D.S. for
additional registration in New Mexico.
This Order is effective November 1,
2021.
Anne Milgram,
Administrator.
[FR Doc. 2021–21424 Filed 9–30–21; 8:45 am]
BILLING CODE 4410–09–P
DEPARTMENT OF JUSTICE
Drug Enforcement Administration
Darryl L. Henry, M.D.; Decision and
Order
On June 4, 2021, the Assistant
Administrator, Diversion Control
Division, Drug Enforcement
Administration (hereinafter,
VerDate Sep<11>2014
18:04 Sep 30, 2021
Jkt 256001
Government), issued an Order to Show
Cause (hereinafter, OSC) to Darryl L.
Henry, M.D. (hereinafter, Registrant) of
Elkhart, Indiana. OSC, at 1. The OSC
proposed the revocation of Registrant’s
Certificate of Registration No.
FH0303292. Id. at 1. It alleged that
Registrant is ‘‘without authority to
handle controlled substances in the
State of Indiana, the state in which
[Registrant is] registered with DEA.’’ Id.
at 2 (citing 21 U.S.C. 824(a)(3)).
Specifically, the OSC alleged that
Registrant’s Indiana medical license was
suspended for 90 days by Order of the
Medical Licensing Board of Indiana,
effective April 22, 2021. Id. The OSC
also alleged that Registrant’s Indiana
controlled substances license expired on
October 31, 2019. Id.
The OSC notified Registrant of the
right to request a hearing on the
allegations or to submit a written
statement, while waiving the right to a
hearing, the procedures for electing each
option, and the consequences for failing
to elect either option. Id. (citing 21 CFR
1301.43). The OSC also notified
Registrant of the opportunity to submit
a corrective action plan. Id. at 3 (citing
21 U.S.C. 824(c)(2)(C)).
Adequacy of Service
In a Declaration dated September 2,
2021, a Diversion Investigator
(hereinafter, the DI) assigned to the
Merrillville, Indiana District Office
stated that on or about June 8, 2021, the
OSC was mailed to both Registrant’s
registered address and his mail-to
address by the DEA Office of Chief
Counsel. Request for Final Agency
Action (hereinafter, RFAA) Exhibit
(hereinafter, RFAAX) 2 (the DI’s
Declaration), at 1–2. The DI stated that
on June 8, 2021, she and a DEA Task
Force Officer attempted to contact
Registrant at his mother’s residence and
spoke with Registrant’s mother. Id. at 2.
According to the DI, Registrant’s mother
stated that Registrant did not live there
and offered to take the OSC and to have
Registrant’s sister contact Registrant
regarding the OSC. Id. The DI stated that
she then left her contact information
with Registrant’s mother. Id. The DI also
stated that on June 8, 2021, she emailed
the OSC to Registrant at the email
address listed in the DEA’s registration
database. Id. According to the DI,
Registrant never responded to the OSC
nor did he request a hearing. Id.
The Government forwarded its RFAA,
along with the evidentiary record, to
this office on September 2, 2021. In its
RFAA, the Government represents that
‘‘more than thirty days have passed
since the [OSC] was served on
[Registrant] and no request for hearing
PO 00000
Frm 00061
Fmt 4703
Sfmt 4703
54479
has been received by DEA.’’ RFAA, at 1.
The Government requests that
Registrant’s DEA registration ‘‘be
revoked and any application for
renewal, or any other applications, [be]
denied, based on [Registrant’s] lack of
state authority.’’ Id. at 5.
Based on the DI’s Declaration, the
Government’s written representations,
and my review of the record, I find that
the Government accomplished service
of the OSC on Registrant on or about
June 8, 2021. I also find that more than
thirty days have now passed since the
Government accomplished service of
the OSC. Further, based on the DI’s
Declaration, the Government’s written
representations, and my review of the
record, I find that neither Registrant, nor
anyone purporting to represent the
Registrant, requested a hearing,
submitted a written statement while
waiving Registrant’s right to a hearing,
or submitted a corrective action plan.
Accordingly, I find that Registrant has
waived the right to a hearing and the
right to submit a written statement and
corrective action plan. 21 CFR
1301.43(d) and 21 U.S.C. 824(c)(2)(C). I,
therefore, issue this Decision and Order
based on the record submitted by the
Government, which constitutes the
entire record before me. 21 CFR
1301.43(e).
Findings of Fact
Registrant’s DEA Registration
Registrant is the holder of DEA
Certificate of Registration No.
FH0303292 at the registered address of
3100 Windsor Ct, Elkhart, IN 46514.
RFAAX 3 (DEA’s online registration
database printout), at 1. Pursuant to this
registration, Registrant is authorized to
dispense controlled substances in
schedules II through V as a practitioner.
Id. Registrant’s registration expires on
October 31, 2021 and is in an ‘‘active
pending’’ status. Id.
The Status of Registrant’s State License
On September 1, 2021, the Medical
Licensing Board of Indiana (hereinafter,
the Board) issued a Summary
Suspension Order (hereinafter, Order)
against Registrant. RFAAX 4, at 1 and 4.
According to the Order, on August 21,
2019, Registrant was charged with two
counts of sexual battery in Elkhart
Superior Court I. Id. at 2. The probable
cause affidavit alleged that on May 7,
2019, the first of two victims saw
Registrant as a patient for a physical
examination, during which Registrant
made inappropriate sexual comments
and unwanted sexual advances on the
victim. Id. at 2–3. Further, the probable
cause affidavit alleged that on May 13,
E:\FR\FM\01OCN1.SGM
01OCN1
54480
Federal Register / Vol. 86, No. 188 / Friday, October 1, 2021 / Notices
2019, a second victim saw Registrant as
a patient for a physical examination,
during which Registrant again made
inappropriate sexual comments and
unwanted sexual advances on the
victim. Id. at 3. The Order concluded
that Registrant ‘‘represents a clear and
immediate danger to the public health
and safety if allowed to continue to
practice as a medical doctor in Indiana.’’
Id. at 4.
Accordingly, the Board ordered that
Registrant’s Indiana medical license,
which had been suspended for 90 days
effective April 22, 2021,1 be summarily
suspended for an additional 90 days,
effective June 24, 2021. Id. The Board
also ordered that the matter would reset
on September 23, 2021 for a hearing to
occur at which the Board would
consider whether the summary
suspension of Registrant’s license
should be extended for an additional 90
days. Id.
According to Indiana’s online records,
of which I take official notice,
Registrant’s Indiana medical license
remains suspended and Registrant’s
controlled substances registration
remains expired.2 https://
www.mylicense.in.gov/everification (last
visited date of signature of this Order).
Accordingly, I find that Registrant is
not currently licensed to engage in the
practice of medicine nor registered to
dispense controlled substances in
Indiana, the state in which Registrant is
registered with the DEA.
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 (hereinafter, 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
1 RFAAX 2, at 2 (the DI’s Declaration). The
Government did not provide documentation for the
original suspension.
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 my finding by filing a
properly supported motion for reconsideration of
finding 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.
VerDate Sep<11>2014
18:04 Sep 30, 2021
Jkt 256001
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 71,371
(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).
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 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, 43 FR
at 27,617.
According to Indiana statute, ‘‘[e]very
person who dispenses or proposes to
dispense any controlled substance
within Indiana must have a registration
issued by the [Indiana Board of
Pharmacy] in accordance with the
board’s rules.’’ Ind. Code § 35–48–3–3(b)
(2021). Further, ‘‘dispense’’ means ‘‘to
deliver a controlled substance to an
ultimate user or research subject by or
pursuant to the lawful order of a
practitioner and includes the
prescribing, administering, packaging,
labeling, or compounding necessary to
prepare the substance for that delivery.’’
Ind. Code § 35–48–1–12 (2021).
Here, the undisputed evidence in the
record is that Registrant currently lacks
authority to dispense controlled
PO 00000
Frm 00062
Fmt 4703
Sfmt 4703
substances in Indiana. As already
discussed, a physician must hold a
controlled substances registration to
dispense a controlled substance in
Indiana. Thus, because Registrant lacks
authority to handle controlled
substances in Indiana, Registrant is not
eligible to maintain a DEA registration.
Accordingly, I 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. FH0303292 issued to
Darryl L. Henry, M.D. 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 application of
Darryl L. Henry, M.D. to renew or
modify this registration, as well as any
other pending application of Darryl L.
Henry, M.D. for additional registration
in Indiana. This Order is effective
November 1, 2021.
Anne Milgram,
Administrator.
[FR Doc. 2021–21425 Filed 9–30–21; 8:45 am]
BILLING CODE 4410–09–P
DEPARTMENT OF JUSTICE
Membership of the Senior Executive
Service and Senior Level Standing
Performance Review Boards
AGENCY:
Department of Justice.
Notice of Department of
Justice’s standing members of the Senior
Executive Service and Senior Level
Performance Review Boards.
ACTION:
Pursuant to agency
regulations, the Department of Justice
announces the membership of its 2021
Senior Executive Service (SES) and
Senior Level (SL) Standing Performance
Review Boards (PRBs). The purpose of
the PRB is to provide fair and impartial
review of SES and SL performance
appraisals; make recommendations to
the appointing authority concerning
performance ratings, performance
awards, and performance-based pay
adjustments; and review and revise, as
appropriate, executive development
plans.
SUMMARY:
FOR FURTHER INFORMATION CONTACT:
Shawn Flinn, Director, Human
Resources, Justice Management
E:\FR\FM\01OCN1.SGM
01OCN1
Agencies
[Federal Register Volume 86, Number 188 (Friday, October 1, 2021)]
[Notices]
[Pages 54479-54480]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2021-21425]
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DEPARTMENT OF JUSTICE
Drug Enforcement Administration
Darryl L. Henry, M.D.; Decision and Order
On June 4, 2021, the Assistant Administrator, Diversion Control
Division, Drug Enforcement Administration (hereinafter, Government),
issued an Order to Show Cause (hereinafter, OSC) to Darryl L. Henry,
M.D. (hereinafter, Registrant) of Elkhart, Indiana. OSC, at 1. The OSC
proposed the revocation of Registrant's Certificate of Registration No.
FH0303292. Id. at 1. It alleged that Registrant is ``without authority
to handle controlled substances in the State of Indiana, the state in
which [Registrant is] registered with DEA.'' Id. at 2 (citing 21 U.S.C.
824(a)(3)).
Specifically, the OSC alleged that Registrant's Indiana medical
license was suspended for 90 days by Order of the Medical Licensing
Board of Indiana, effective April 22, 2021. Id. The OSC also alleged
that Registrant's Indiana controlled substances license expired on
October 31, 2019. Id.
The OSC notified Registrant of the right to request a hearing on
the allegations or to submit a written statement, while waiving the
right to a hearing, the procedures for electing each option, and the
consequences for failing to elect either option. Id. (citing 21 CFR
1301.43). The OSC also notified Registrant of the opportunity to submit
a corrective action plan. Id. at 3 (citing 21 U.S.C. 824(c)(2)(C)).
Adequacy of Service
In a Declaration dated September 2, 2021, a Diversion Investigator
(hereinafter, the DI) assigned to the Merrillville, Indiana District
Office stated that on or about June 8, 2021, the OSC was mailed to both
Registrant's registered address and his mail-to address by the DEA
Office of Chief Counsel. Request for Final Agency Action (hereinafter,
RFAA) Exhibit (hereinafter, RFAAX) 2 (the DI's Declaration), at 1-2.
The DI stated that on June 8, 2021, she and a DEA Task Force Officer
attempted to contact Registrant at his mother's residence and spoke
with Registrant's mother. Id. at 2. According to the DI, Registrant's
mother stated that Registrant did not live there and offered to take
the OSC and to have Registrant's sister contact Registrant regarding
the OSC. Id. The DI stated that she then left her contact information
with Registrant's mother. Id. The DI also stated that on June 8, 2021,
she emailed the OSC to Registrant at the email address listed in the
DEA's registration database. Id. According to the DI, Registrant never
responded to the OSC nor did he request a hearing. Id.
The Government forwarded its RFAA, along with the evidentiary
record, to this office on September 2, 2021. In its RFAA, the
Government represents that ``more than thirty days have passed since
the [OSC] was served on [Registrant] and no request for hearing has
been received by DEA.'' RFAA, at 1. The Government requests that
Registrant's DEA registration ``be revoked and any application for
renewal, or any other applications, [be] denied, based on
[Registrant's] lack of state authority.'' Id. at 5.
Based on the DI's Declaration, the Government's written
representations, and my review of the record, I find that the
Government accomplished service of the OSC on Registrant on or about
June 8, 2021. I also find that more than thirty days have now passed
since the Government accomplished service of the OSC. Further, based on
the DI's Declaration, the Government's written representations, and my
review of the record, I find that neither Registrant, nor anyone
purporting to represent the Registrant, requested a hearing, submitted
a written statement while waiving Registrant's right to a hearing, or
submitted a corrective action plan. Accordingly, I find that Registrant
has waived the right to a hearing and the right to submit a written
statement and corrective action plan. 21 CFR 1301.43(d) and 21 U.S.C.
824(c)(2)(C). I, therefore, issue this Decision and Order based on the
record submitted by the Government, which constitutes the entire record
before me. 21 CFR 1301.43(e).
Findings of Fact
Registrant's DEA Registration
Registrant is the holder of DEA Certificate of Registration No.
FH0303292 at the registered address of 3100 Windsor Ct, Elkhart, IN
46514. RFAAX 3 (DEA's online registration database printout), at 1.
Pursuant to this registration, Registrant is authorized to dispense
controlled substances in schedules II through V as a practitioner. Id.
Registrant's registration expires on October 31, 2021 and is in an
``active pending'' status. Id.
The Status of Registrant's State License
On September 1, 2021, the Medical Licensing Board of Indiana
(hereinafter, the Board) issued a Summary Suspension Order
(hereinafter, Order) against Registrant. RFAAX 4, at 1 and 4. According
to the Order, on August 21, 2019, Registrant was charged with two
counts of sexual battery in Elkhart Superior Court I. Id. at 2. The
probable cause affidavit alleged that on May 7, 2019, the first of two
victims saw Registrant as a patient for a physical examination, during
which Registrant made inappropriate sexual comments and unwanted sexual
advances on the victim. Id. at 2-3. Further, the probable cause
affidavit alleged that on May 13,
[[Page 54480]]
2019, a second victim saw Registrant as a patient for a physical
examination, during which Registrant again made inappropriate sexual
comments and unwanted sexual advances on the victim. Id. at 3. The
Order concluded that Registrant ``represents a clear and immediate
danger to the public health and safety if allowed to continue to
practice as a medical doctor in Indiana.'' Id. at 4.
Accordingly, the Board ordered that Registrant's Indiana medical
license, which had been suspended for 90 days effective April 22,
2021,\1\ be summarily suspended for an additional 90 days, effective
June 24, 2021. Id. The Board also ordered that the matter would reset
on September 23, 2021 for a hearing to occur at which the Board would
consider whether the summary suspension of Registrant's license should
be extended for an additional 90 days. Id.
---------------------------------------------------------------------------
\1\ RFAAX 2, at 2 (the DI's Declaration). The Government did not
provide documentation for the original suspension.
---------------------------------------------------------------------------
According to Indiana's online records, of which I take official
notice, Registrant's Indiana medical license remains suspended and
Registrant's controlled substances registration remains expired.\2\
https://www.mylicense.in.gov/everification (last visited date of
signature of this Order).
---------------------------------------------------------------------------
\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 my finding by filing
a properly supported motion for reconsideration of finding 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].
---------------------------------------------------------------------------
Accordingly, I find that Registrant is not currently licensed to
engage in the practice of medicine nor registered to dispense
controlled substances in Indiana, the state in which Registrant is
registered with the DEA.
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 (hereinafter, 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 71,371 (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).
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 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, 43
FR at 27,617.
According to Indiana statute, ``[e]very person who dispenses or
proposes to dispense any controlled substance within Indiana must have
a registration issued by the [Indiana Board of Pharmacy] in accordance
with the board's rules.'' Ind. Code Sec. 35-48-3-3(b) (2021). Further,
``dispense'' means ``to deliver a controlled substance to an ultimate
user or research subject by or pursuant to the lawful order of a
practitioner and includes the prescribing, administering, packaging,
labeling, or compounding necessary to prepare the substance for that
delivery.'' Ind. Code Sec. 35-48-1-12 (2021).
Here, the undisputed evidence in the record is that Registrant
currently lacks authority to dispense controlled substances in Indiana.
As already discussed, a physician must hold a controlled substances
registration to dispense a controlled substance in Indiana. Thus,
because Registrant lacks authority to handle controlled substances in
Indiana, Registrant is not eligible to maintain a DEA registration.
Accordingly, I 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.
FH0303292 issued to Darryl L. Henry, M.D. 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 application of Darryl L. Henry, M.D. to renew or
modify this registration, as well as any other pending application of
Darryl L. Henry, M.D. for additional registration in Indiana. This
Order is effective November 1, 2021.
Anne Milgram,
Administrator.
[FR Doc. 2021-21425 Filed 9-30-21; 8:45 am]
BILLING CODE 4410-09-P