Kamal Tiwari, M.D.; Pain Management and Surgery Center of Southern Indiana; Decision and Order, 71604-71607 [2011-29708]
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[FR Doc. 2011–29809 Filed 11–17–11; 8:45 am]
BILLING CODE P
DEPARTMENT OF JUSTICE
Drug Enforcement Administration
[Docket No. 10–53]
Kamal Tiwari, M.D.; Pain Management
and Surgery Center of Southern
Indiana; Decision and Order
On April 23, 2010, I, the
Administrator of the Drug Enforcement
Administration, issued an Order to
Show Cause and Immediate Suspension
of Registration to Kamal Tiwari, M.D.
(Respondent Tiwari), holder of DEA
Certificate of Registration BT2936411,
and his principal place of business, the
Pain Management and Surgery Center
(Respondent PMSC), holder of DEA
Certificate of Registration BP4917413,
both of Bloomington, Indiana. The
Show Cause Order proposed the
revocation of each Respondent’s
registration, on the ground that
Respondent Tiwari had committed acts
which render the continued registration
of each Respondent ‘‘inconsistent with
the public interest.’’ Show Cause Order,
at 1 (citing 21 U.S.C. 823(f) and
824(a)(4)).
The Show Cause Order specifically
alleged that between March 2003 and
August 2008, Respondent Tiwari issued
‘‘numerous’’ prescriptions for controlled
substances to three patients, who were
addicts, and ‘‘who did not exhibit any
verifiable medical indications
warranting the prescribing of controlled
substances.’’ Id. at 2. The Order thus
alleged that Respondent lacked a
legitimate medical purpose and acted
outside the usual course of professional
practice in issuing the prescriptions and
violated federal and state laws. Id.
(citing 21 U.S.C. 841(a)(1); 21 CFR
1306.04(a); Ind. Code § 25–1–9–4(a)(9)).
With respect to these patients, the Show
Cause Order further alleged that
Respondent prescribed controlled
substances to them ‘‘in exchange for
their agreements to undergo medical
procedures * * * for profit,’’ and that
‘‘[t]his prescribing pattern indicates’’
that he issued the ‘‘prescriptions
without a legitimate medical purpose
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and outside the scope of professional
practice.’’ Id. at 2–3.
The Show Cause Order also alleged
that a medical expert concluded that
Respondent’s prescribing to these three
patients lacked ‘‘a legitimate medical
purpose and [was] outside the scope of
professional practice.’’ Id. at 3. The
Order further alleged that the expert
concluded with respect to these three
patients, as well as nine other patients,
that Respondent’s ‘‘actions encouraged
the abuse of controlled substances and
allowed their misuse,’’ that his
prescribing of controlled substances
contributed to the deaths of six patients,
and that there was no justification for
his ‘‘long-term prescribing of controlled
substances * * * or the administration
of procedures using controlled
substances’’ to these patients. Id.
Next, the Show Cause Order alleged
that a second medical expert concluded
that Respondent Tiwari had prescribed
controlled substances to, and/or
performed medical procedures using
controlled substances without medical
justification on, several other patients.
Id. Finally, the Show Cause Order
alleged that ‘‘at least nine of’’
Respondent’s patients had died over a
six-year period, the most recent being in
February 2009, and that Respondent had
‘‘continue[d] to prescribe controlled
substances to patients at per-patient
rates that [we]re similar to the
prescribing rates in 2008, when two of
[his] patients died of conditions related
to drug abuse.’’ Id.
Based on the above, I concluded that
Respondents’ continued registration
during the pendency of the proceeding
‘‘constitutes an imminent danger to the
public health and safety.’’ Id. at 4. I
therefore ordered that each
Respondent’s registration be
immediately suspended. Id.
On May 24, 2010, Respondents filed
a request for a hearing and the matter
was assigned to an Administrative Law
Judge (ALJ), who proceeded to conduct
pre-hearing procedures. However, on
May 27, 2010, the Government moved
for Summary Disposition and filed a
Motion to Stay the Filing of Prehearing
Statements. Mot. Summ. Disp., at 2–3.
The basis of the Government’s motion
was that each Respondent currently
lacks authority to handle controlled
substances in the State of Indiana, the
jurisdiction where the Respondents are
licensed to practice medicine and hold
their DEA registrations. Mot. Summ.
Disp., at 1–2 (citing 21 U.S.C. 801(21),
823(f), 824(a)(3)). In support of its
motion, the Government attached a
letter from the Medical Licensing Board
of Indiana (MLB) to Respondent Kamal
Tiwari, dated May 26, 2010, stating that
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his Indiana controlled substance
registration (CSR) Number 01034945B,
had been suspended pursuant to
Indiana Code § 35–48–3–5(e).1 Id. at Ex.
3. The Government also attached a
printout from the Indiana Online
Licensing Web site which shows that
Indiana CSR Number 61100223B, held
by Respondent PMSC, has also been
suspended. Id. at Ex. 4.
Thereafter, the ALJ issued an Order
for Respondents’ Response to
Government’s Motion for Summary
Disposition and to Stay the Filing of
Prehearing Statements; she also stayed
the filing of the Prehearing statements.
ALJ’s Recommended Ruling (also ALJ),
at 4.
On June 16, 2010, Respondents filed
their Response. Therein, Respondents
argued that granting summary
disposition based on their lack of state
authority to handle controlled
substances would be circular and
violate their right to Due Process,
because the State’s suspension of their
state CSRs was based on the DEA Order
to Show Cause and Immediate
Suspension of Registration. Resps.
Response at 1, 3–6. Respondents also
argued that in suspending their state
registrations, the MLB cited ‘‘no basis
for the State suspension other than the
federal suspension.’’ Id. at 2.
Respondents further maintain that the
MLB ‘‘has no authority concerning
controlled substances registrations,
which are instead under the jurisdiction
of the Indiana State Board of
Pharmacy.’’ Id. at 2–3 (citations
omitted).
Respondents also argued that in none
of the cases cited by the Government
did it ‘‘attempt to rely * * * on a
derivative state action triggered by the
Government’s suspension,’’ and that
‘‘[n]ot a single one of the Government’s
cases revoke[d] a registration under 21
U.S.C. 843(a)(3) without some
independent determination’’ by the
respective state authority. Id. at 4.
Respondents thus maintained that
‘‘[d]epriving a practitioner of the right to
review of a DEA action based solely on
a State suspension that was in turn
based solely on the original DEA action
would violate Due Process.’’ Id. at 5.
Finally, Respondents also contended
that ‘‘[p]ractitioners may not be able to
obtain review of either suspension, if
the State takes the same position that
the [DEA] does here.’’ Id.
1 This provision states: ‘‘If the Drug Enforcement
Administration terminates, denies, suspends or
revokes a federal registration for the manufacture,
distribution, or dispensing of controlled substances,
a registration issued by the board under this chapter
is automatically suspended.’’ Ind. Code § 35–48–3–
5(e).
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On June 17, the Government filed its
Reply to Opposition to Government’s
Motion for Summary Disposition and to
Stay the Filing of Pre-hearing
Statements (Reply). The Government
argued that ‘‘Indiana law specifically
provides a basis for substantive review
of any state suspension which is
triggered by a DEA suspension.’’ Reply
at 1 (citing Ind. Code § 35–48–3–5(f)).2
The Government further argues that
under DEA precedent, ‘‘when a state
suspends a respondent’s controlled
substance privileges, Federal revocation
is warranted as long as the respondent
has some mechanism to challenge the
state action.’’ Id. at 2 (citing Odette
Louise Campbell, M.D., No. 09–62,
Order Remanding for Further
Proceedings).3
On June 18, 2010, Respondents filed
a Surreply in Opposition to
Government’s Motion for Summary
Disposition (Surreply), in which they
assert that the Government
‘‘fundamentally misunderstands the
Indiana statutory scheme.’’ Surreply, at
1. Therein, the Respondents again
argued that the ‘‘Government’s Motion
for Summary Disposition should be
denied because it relies on a potential,
nonbinding state hearing, a theoretical
possibility that cannot be triggered until
the Indiana Board that actually has
authority to suspend the Respondents’
controlled substances registrations
issues an order to show cause, which it
has not.’’ Id. Respondents further
maintained that ‘‘the Indiana Advisory
Committee could avoid the hearing
provision on which the Government
relies solely by not issuing the show
cause notice.’’ Id. at 2.
On June 21, 2010, the ALJ issued an
Order for Government’s Response to
Surreply in Opposition to Government’s
Motion for Summary Disposition. On
July 2, 2010, the Government filed its
Response to Surreply. The Government
reiterated that the Respondents’ Indiana
CSRs have been suspended and that
2 ‘‘The board may reinstate a registration that has
been suspended under subsection (e), after a
hearing, if the board is satisfied that the applicant
is able to manufacture, distribute, or dispense
controlled substances with reasonable skill and
safety to the public.’’ Ind. Code § 35–48–3–5(f).
3 The Government also argued that ‘‘to the extent
that Respondents argue that the Medical Licensing
Board of Indiana * * * has no authority concerning
controlled substance registrations, that
jurisdictional argument must be made to the Board
of Pharmacy,’’ and that in ‘‘its letter to [Respondent]
Tiwari, the Medical Licensing Board * * * merely
informed Respondent that his CSR was suspended
pursuant to the appropriate statute.’’ Reply at 3.
Finally, the Government attached a May 27, 2010
letter from the Indiana Board of Pharmacy to
Respondents which stated that Indiana CSR
Number 61100223B, which is held by Respondent
PMSC, had been suspended pursuant to Ind. Code
§ 35–48–3–5(e). Reply at 3, Ex. 3–A.
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while the issuance of the DEA
Immediate Suspension Orders ‘‘may
have been the cause of the state
suspension, [they] do not govern
whether those state suspensions remain
in effect.’’ Response to Surreply, at 1.
The Government again argued that
under Indiana law, the Board of
Pharmacy ‘‘ ‘may reinstate a [CSR] that
has been suspended under subsection
(e), after a hearing, if the board is
satisfied that the applicant is able to
* * * dispense controlled substances
with reasonable skill and safety to the
public.’ ’’ Id. (quoting Ind. Code § 35–
48–3–5(f)). The Government also noted
that Respondents had filed a Petition for
Review of the state suspensions, albeit
with the Medical Licensing Board and
not the Board of Pharmacy. Id. The
Government argued that this
nonetheless demonstrated that
Respondents knew of, and were
pursuing, their right to seek
administrative review of the State’s
suspensions, pursuant to section 35–48–
3–5(f).
Next, the Government argued that
Respondents’ contention that Indiana
must issue an Order to Show Cause
prior to suspending their CSRs is
without merit, and that in any case, the
issue is a matter of state law, and not a
matter for a DEA ALJ to decide.
Response to Surreply, at 2. Finally, the
Government argued that the
Respondents’ interpretation of the
Indiana statutes would render them
inconsistent and meaningless. Id. at 2–
3.
On July 7, 2010, the ALJ issued her
recommended decision (hereinafter
ALJ). Therein, the ALJ specifically
found that the Indiana Board of
Pharmacy had automatically suspended
the Indiana CSRs held by the
Respondents. ALJ at 5. Noting the
settled Agency rule that ‘‘possessing
authority under state law to handle
controlled substances is an essential
condition for holding a DEA
registration,’’ id. at 6 (quoting Joseph
Baumstarck, M. D., 74 FR 17525, 17527
(2009)), and rejecting Respondents’
contention that granting summary
disposition would deny them their right
to Due Process, the ALJ granted the
Government’s Motion for Summary
Disposition. ALJ at 5–7, 9. The ALJ thus
recommended that I revoke the
Respondents’ DEA Certificates of
Registration and deny any pending
applications to renew their registrations.
Id. at 9.
Neither party filed exceptions to the
ALJ’s decision. Thereafter, the record
was forwarded to me for final agency
action.
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Having considered the record as a
whole including the parties’ pleadings,
I adopt the ALJ’s findings of fact and
recommended sanction. I will therefore
revoke Respondents’ respective DEA
Certificates of Registration and deny any
pending applications to renew their
registrations. I make the following
findings.
Findings
Respondent Tiwari is the holder of
Certificate of Registration BT2936411,
which authorizes him to dispense
controlled substances in schedules II
through V, as a practitioner. While this
registration was due to expire on
November 30, 2009, on October 2, 2009,
Respondent Tiwari submitted a timely
renewal application. Respondent
Tiwari’s registration thus remains
active, albeit in suspended status,
pending the issuance of the Final Order
in this matter. 5 U.S.C. 558(c).
Respondent PMSC is the holder of
Certificate of Registration BP4917413,
which authorizes it to dispense
controlled substances in schedules II
through V, as a hospital/clinic. This
registration is due to expire on March
31, 2011. According to the registration
records of this Agency, Respondent
Tiwari has also submitted an
application to renew Respondent
PMSC’s registration.
On or about May 27, 2010, the Indiana
Board of Pharmacy placed Respondent
PMSC’s Indiana CSR in suspended
status. See Reply to Opp. to Gov. Mot.
for Summ. Disp., at Ex. 3–A. Moreover,
according to a letter from the MLB to
Respondent Tiwari, on or about May 26,
2010, his Indiana CSR was placed in
suspended status. Id. at Ex. 3. According
to the Indiana Online Licensing Web
site, of which I take official notice, each
Respondent’s CSR remains suspended
as of the date of this Decision and Final
Order.4
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Discussion
Under the Controlled Substances Act
(CSA), a practitioner must be currently
authorized to handle controlled
substances in ‘‘the jurisdiction in which
he practices’’ in order to maintain a
DEA registration. See 21 U.S.C. 802(21)
4 Under the Administrative Procedure Act (APA),
an agency ‘‘may take official notice of facts at any
stage in a proceeding-even in the final decision.’’
U.S. Dept. of Justice, Attorney General’s Manual on
the Administrative Procedure Act 80 (1947) (Wm.
W. Gaunt & Sons, Inc., Reprint 1979). In accordance
with the APA and DEA’s regulations, Respondent
is ‘‘entitled on timely request, to an opportunity to
show to the contrary.’’ 5 U.S.C. 556(e); see also 21
CFR 1316.59(e). Respondent can dispute the facts
of which I take official notice by filing a properly
supported motion for reconsideration within twenty
days of service of this Order, which shall begin on
the date it is mailed.
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(‘‘[t]he term ‘practitioner’ means a
physician * * * pharmacy, hospital, 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’’). See
also id. § 823(f) (‘‘The Attorney General
shall register practitioners * * * if the
applicant is authorized to dispense
* * * controlled substances under the
laws of the State in which he
practices.’’). As these provisions make
plain, possessing authority under state
law to handle controlled substances is
an essential condition for obtaining and
maintaining a practitioner’s registration.
Accordingly, DEA has held that
revocation of a practitioner’s registration
is warranted whenever his (or its) state
authority to dispense controlled
substances has been suspended or
revoked. David W. Wang, 72 FR 54297,
54298 (2007); Sheran Arden Yeates, 71
FR 39130, 39131 (2006); Dominick A.
Ricci, 58 FR 51104, 51105 (1993); Bobby
Watts, 53 FR 11919, 11920 (1988). See
also 21 U.S.C. 824(a)(3) (authorizing
revocation of a registration ‘‘upon a
finding that the registrant * * * has had
his State license or registration
suspended [or] revoked * * * and is no
longer authorized by State law to engage
in the * * * distribution [or] dispensing
of controlled substances’’).
DEA has further held that revocation
is warranted even where a practitioner’s
state authority has been summarily
suspended and the State has yet to
provide the practitioner with a hearing
to challenge the State’s action and at
which he (or it) may ultimately prevail.
See Robert Wayne Mosier, 75 FR 49950
(2010) (‘‘revocation is warranted * * *
even in those instances where a
practitioner’s state license has only been
suspended, and there is the possibility
of reinstatement’’); accord Bourne
Pharmacy, 72 FR 18273, 18274 (2007);
Anne Lazar Thorn, 62 FR 12847 (1997).
Here, it is undisputed that the State
has suspended the state controlled
substance registration of each
Respondent. DEA has long held that the
order of a state agency suspending or
revoking a practitioner’s state authority
cannot be collaterally attacked in a
proceeding under the CSA. See Hicham
K. Riba, 73 FR 75773, 75774 (2008)
(rejecting claim that state proceeding
was fundamentally unfair based on
alleged improper ex parte influence of
director of state board as ‘‘not
addressable in’’ DEA proceeding); Sunil
Bhasin, 72 FR at 5082, 5083 (2007)
(rejecting claim that settlement
agreement in which Respondent
surrendered state license was produced
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by fraud and was unconscionable; ‘‘a
DEA Show Cause Proceeding is not the
proper forum to litigate the issue’’); see
also Shahid Musud Siddiqui, 61 FR
14818 (1996); Robert A. Leslie, 60 FR
14004 (1995).
The underlying premise of these cases
is that the States exercise sovereign
powers in regulating the medical
profession and that challenges to the
validity of state board orders should be
raised and litigated in state forums. See,
e.g., Riba, 73 FR at 75774 (claim that
‘‘state proceeding was fundamentally
unfair * * * is not addressable in’’ DEA
proceeding). These cases likewise
implicitly recognize that state boards
and state courts are fully cognizant of
their obligation under the Due Process
Clause to provide a full and fair
opportunity to litigate the issues. Cf.
University of Tennessee v. Elliott, 478
U.S. 788, 797–98 (1986) (‘‘When an
administrative agency is acting in a
judicial capacity and resolves disputed
issues of fact properly before it which
the parties have had an adequate
opportunity to litigate, the courts have
not hesitated to apply res judicata[.]’’)
(int. quotations and citations omitted).
It is true that in Odette Louise
Campbell, M.D., No. 09–62, I denied the
Government’s request for a final order
based on the registrant’s loss of her
controlled substance prescribing
authority under Texas law where the
State had suspended that authority
based on DEA’s issuance of an
immediate suspension order and
remanded the matter for further
proceedings. Campbell, Order
Remanding for Further Proceedings, at
10–11. However, I noted that specific
provisions of Texas law and regulations
suggested that the registrant was not
entitled to a hearing to challenge the
merits of the state suspension because it
was based on the DEA immediate
suspension. Id. at 9 (citing Texas Health
& Safety Code §§ 481.063(e)(3),
481.063(h), 481.066(g), and Tex. Admin.
Code § 13.272(h)). Moreover, I ordered
the ALJ to first determine whether the
State had provided, or would provide,
the registrant with a hearing; I further
ordered that if the State had provided or
would provide a hearing, the
Government could renew its motion for
summary disposition. Id. at 10.
By contrast, while the Indiana
Board(s) suspended Respondents’ state
registrations based on the state law
provision that ‘‘[i]f the Drug
Enforcement Administration * * *
suspends * * * a federal registration for
the * * * dispensing of controlled
substances, a registration issued by the
board under this chapter is
automatically suspended,’’ Ind. Code
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§ 35–48–3–5(e), state law further
provides that ‘‘[t]he board may reinstate
a registration that has been suspended
under subsection(e) after a hearing, if
the board is satisfied that the applicant
is able to manufacture, distribute or
dispense controlled substances with
reasonable skill and safety to the
public.’’ Id. § 35–48–3–5(f). (emphasis
added). Thus, it appears that
Respondents are entitled to a hearing to
challenge the underlying allegations
before the State board.
Respondents contend that their right
to a hearing under section 35–48–3–5(f)
‘‘is not triggered until the Indiana
Controlled Substances Advisory
Committee serves upon the * * *
registrant an order to show cause why
registration should not be denied,
revoked or suspended,’’ and that
‘‘absent such a step, the purported
suspension issued by the board * * * is
a nullity, and cannot form the basis for
a federal suspension.’’ Surreply at 2
(citing Ind. Code § 35–48–3–6(a)).5
Respondents further argue that ‘‘[i]f it
could, then the Indiana Advisory
Committee could avoid the hearing
provision on which the Government
relies solely by not issuing the show
cause notice.’’ Id.
Beyond the fact that Respondents’
argument appears to be based on the
speculative premise that the Indiana
authorities will attempt to prevent them
from obtaining a hearing, the Indiana
statute makes clear that Respondents are
entitled to a hearing. Presumably, the
Indiana courts are open and can provide
an appropriate remedy in the event the
state board refuses to provide
Respondents with a hearing. See Ind.
Code § 34–27–3–1 (‘‘An action for
mandate may be prosecuted against any
inferior tribunal * * * public * * *
officer, or person to compel the
performance of any * * * act that the
law specifically requires[.]’’).
Moreover, the question of whether the
Indiana suspensions are a nullity
because the State did not serve
Respondents with a Show Cause Order
is an issue of state law and for the
Indiana courts to decide. As such, it is
outside the scope of this proceeding.
See George S. Heath, M.D., 51 FR 26610
(1986) (‘‘DEA accepts as valid and
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5 This
provision states:
Before recommending a denial, suspension, or
revocation of a registration, or before refusing a
renewal of registration, the board shall serve upon
the applicant or registrant an order to show cause
why registration should not be denied, revoked, or
suspended * * *. The order to show cause shall
contain a statement of the basis therefor [sic] and
shall call upon the applicant or registrant to appear
before the board at a time and place not less than
thirty (30) days after the date of service of the order
* * *.
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lawful the action of a state regulatory
board unless that action is overturned
by a state court or otherwise pursuant to
state law. * * * The [DEA] will not
consider a challenge to the lawfulness of
a Georgia Board Order. Such a challenge
must be made in another forum.’’); see
also Shahid Musud Siddiqui, M.D., 61
FR 14818, 14818–19 (DEA 1996) (A
‘‘DEA administrative proceeding is not
an appropriate forum for wholesale
review of state criminal and
administrative actions taken by the State
of New York arising out of the laws of
the State of New York. To allow it to be
so would be to permit a wide collateral
attack upon such convictions.’’) (int.
quotations and citation omitted).
Finally, Respondents argue that the
suspensions of their state CSRs are
invalid because they were suspended by
the MLB and only the Pharmacy Board
has authority under state law to suspend
their registrations. However, the
Pharmacy Board’s May 27, 2010 letter
makes clear that it (and not the MLB)
was suspending Respondent PMSC’s
registration, and even if Respondent
Tiwari’s controlled substance
registration was suspended by the MLB,
the validity of this action is also a
question of state law and for the Indiana
courts to decide. Riba, 73 FR at 75774;
Heath, 51 FR at 26610.
Because there is no dispute over the
material fact that each Respondent’s
Indiana controlled substance
registration has been suspended, each is
without authority to hold a DEA
registration.6 See 21 U.S.C. 802(21).
Accordingly, Respondents’ registrations
will be revoked and any pending
applications will be denied.
Order
Pursuant to the authority vested in me
by 21 U.S.C. 823(f) and 824(a), as well
as 28 CFR 0.100(b) and 0.104, I order
that DEA Certificate of Registration,
BT2936411, issued to Respondent
Kamal Tiwari, M.D., and DEA
Certificate of Registration, BP4917413,
issued to Respondent Pain Management
and Surgery Center of Southern Indiana,
be, and they hereby are, revoked. I
further order that any pending
applications of Kamal Tiwari, M.D. and
Pain Management and Surgery Center of
Southern Indiana, to renew or modify
such registrations, be, and they hereby
6 Where, as here, no material fact is in dispute,
there is no need for an evidentiary hearing and
summary disposition is appropriate. See Michael G.
Dolin, M.D., 65 FR 5661 (2000); see also Philip E.
Kirk, M.D., 48 FR 32887 (1983), aff’d sub nom Kirk
v. Mullen, 749 F.2d 297 (6th Cir. 1984).
PO 00000
Frm 00098
Fmt 4703
Sfmt 4703
71607
are, denied. This Order is effective
immediately.7
Dated: November 8, 2011.
Michele M. Leonhart,
Administrator.
[FR Doc. 2011–29708 Filed 11–17–11; 8:45 am]
BILLING CODE 4410–09–P
DEPARTMENT OF JUSTICE
Federal Bureau of Investigation
[OMB Number 1110–0008]
Agency Information Collection
Activities: Proposed Collection,
Comments Requested; Extension of a
Currently Approved Collection;
Monthly Return of Arson Offenses
Known to Law Enforcement
30-day Notice of Information
Collection Under Review.
ACTION:
The Department of Justice, Federal
Bureau of Investigation, Criminal Justice
Information Services Division (CJIS)
will be submitting the following
information collection request to the
Office of Management and Budget
(OMB) for review and clearance in
accordance with established review
procedures of the Paperwork Reduction
Act of 1995. The proposed information
collection is published to obtain
comments from the public and affected
agencies. This proposed information
collection was previously published in
the Federal Register on September 15,
2011, Volume 76, Number 179, Page
57081, allowing for a 60 day comment
period.
The purpose of this notice is to allow
for an additional 30 days for public
comment until December 19, 2011. This
process is conducted in accordance with
5 CFR 1320.10.
Written comments and/or suggestions
regarding the items contained in this
notice, especially the estimated public
burden and associated response time,
should be directed to Mr. Gregory E.
Scarbro, Unit Chief, Federal Bureau of
Investigation, CJIS Division, Module
E–3, 1000 Custer Hollow Road,
Clarksburg, West Virginia 26306;
facsimile (304) 625–3566.
Written comments and suggestions
from the public and affected agencies
concerning the proposed collection of
information are encouraged. Comments
should address one or more of the
following four points:
7 For the same reason that I ordered that the
Respondents’ registration be immediately
suspended, I conclude that the public interest
necessitates that this Order be effective
immediately. See 21 CFR 1316.67.
E:\FR\FM\18NON1.SGM
18NON1
Agencies
[Federal Register Volume 76, Number 223 (Friday, November 18, 2011)]
[Notices]
[Pages 71604-71607]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2011-29708]
-----------------------------------------------------------------------
DEPARTMENT OF JUSTICE
Drug Enforcement Administration
[Docket No. 10-53]
Kamal Tiwari, M.D.; Pain Management and Surgery Center of
Southern Indiana; Decision and Order
On April 23, 2010, I, the Administrator of the Drug Enforcement
Administration, issued an Order to Show Cause and Immediate Suspension
of Registration to Kamal Tiwari, M.D. (Respondent Tiwari), holder of
DEA Certificate of Registration BT2936411, and his principal place of
business, the Pain Management and Surgery Center (Respondent PMSC),
holder of DEA Certificate of Registration BP4917413, both of
Bloomington, Indiana. The Show Cause Order proposed the revocation of
each Respondent's registration, on the ground that Respondent Tiwari
had committed acts which render the continued registration of each
Respondent ``inconsistent with the public interest.'' Show Cause Order,
at 1 (citing 21 U.S.C. 823(f) and 824(a)(4)).
The Show Cause Order specifically alleged that between March 2003
and August 2008, Respondent Tiwari issued ``numerous'' prescriptions
for controlled substances to three patients, who were addicts, and
``who did not exhibit any verifiable medical indications warranting the
prescribing of controlled substances.'' Id. at 2. The Order thus
alleged that Respondent lacked a legitimate medical purpose and acted
outside the usual course of professional practice in issuing the
prescriptions and violated federal and state laws. Id. (citing 21
U.S.C. 841(a)(1); 21 CFR 1306.04(a); Ind. Code Sec. 25-1-9-4(a)(9)).
With respect to these patients, the Show Cause Order further alleged
that Respondent prescribed controlled substances to them ``in exchange
for their agreements to undergo medical procedures * * * for profit,''
and that ``[t]his prescribing pattern indicates'' that he issued the
``prescriptions without a legitimate medical purpose and outside the
scope of professional practice.'' Id. at 2-3.
The Show Cause Order also alleged that a medical expert concluded
that Respondent's prescribing to these three patients lacked ``a
legitimate medical purpose and [was] outside the scope of professional
practice.'' Id. at 3. The Order further alleged that the expert
concluded with respect to these three patients, as well as nine other
patients, that Respondent's ``actions encouraged the abuse of
controlled substances and allowed their misuse,'' that his prescribing
of controlled substances contributed to the deaths of six patients, and
that there was no justification for his ``long-term prescribing of
controlled substances * * * or the administration of procedures using
controlled substances'' to these patients. Id.
Next, the Show Cause Order alleged that a second medical expert
concluded that Respondent Tiwari had prescribed controlled substances
to, and/or performed medical procedures using controlled substances
without medical justification on, several other patients. Id. Finally,
the Show Cause Order alleged that ``at least nine of'' Respondent's
patients had died over a six-year period, the most recent being in
February 2009, and that Respondent had ``continue[d] to prescribe
controlled substances to patients at per-patient rates that [we]re
similar to the prescribing rates in 2008, when two of [his] patients
died of conditions related to drug abuse.'' Id.
Based on the above, I concluded that Respondents' continued
registration during the pendency of the proceeding ``constitutes an
imminent danger to the public health and safety.'' Id. at 4. I
therefore ordered that each Respondent's registration be immediately
suspended. Id.
On May 24, 2010, Respondents filed a request for a hearing and the
matter was assigned to an Administrative Law Judge (ALJ), who proceeded
to conduct pre-hearing procedures. However, on May 27, 2010, the
Government moved for Summary Disposition and filed a Motion to Stay the
Filing of Prehearing Statements. Mot. Summ. Disp., at 2-3.
The basis of the Government's motion was that each Respondent
currently lacks authority to handle controlled substances in the State
of Indiana, the jurisdiction where the Respondents are licensed to
practice medicine and hold their DEA registrations. Mot. Summ. Disp.,
at 1-2 (citing 21 U.S.C. 801(21), 823(f), 824(a)(3)). In support of its
motion, the Government attached a letter from the Medical Licensing
Board of Indiana (MLB) to Respondent Kamal Tiwari, dated May 26, 2010,
stating that
[[Page 71605]]
his Indiana controlled substance registration (CSR) Number 01034945B,
had been suspended pursuant to Indiana Code Sec. 35-48-3-5(e).\1\ Id.
at Ex. 3. The Government also attached a printout from the Indiana
Online Licensing Web site which shows that Indiana CSR Number
61100223B, held by Respondent PMSC, has also been suspended. Id. at Ex.
4.
---------------------------------------------------------------------------
\1\ This provision states: ``If the Drug Enforcement
Administration terminates, denies, suspends or revokes a federal
registration for the manufacture, distribution, or dispensing of
controlled substances, a registration issued by the board under this
chapter is automatically suspended.'' Ind. Code Sec. 35-48-3-5(e).
---------------------------------------------------------------------------
Thereafter, the ALJ issued an Order for Respondents' Response to
Government's Motion for Summary Disposition and to Stay the Filing of
Prehearing Statements; she also stayed the filing of the Prehearing
statements. ALJ's Recommended Ruling (also ALJ), at 4.
On June 16, 2010, Respondents filed their Response. Therein,
Respondents argued that granting summary disposition based on their
lack of state authority to handle controlled substances would be
circular and violate their right to Due Process, because the State's
suspension of their state CSRs was based on the DEA Order to Show Cause
and Immediate Suspension of Registration. Resps. Response at 1, 3-6.
Respondents also argued that in suspending their state registrations,
the MLB cited ``no basis for the State suspension other than the
federal suspension.'' Id. at 2. Respondents further maintain that the
MLB ``has no authority concerning controlled substances registrations,
which are instead under the jurisdiction of the Indiana State Board of
Pharmacy.'' Id. at 2-3 (citations omitted).
Respondents also argued that in none of the cases cited by the
Government did it ``attempt to rely * * * on a derivative state action
triggered by the Government's suspension,'' and that ``[n]ot a single
one of the Government's cases revoke[d] a registration under 21 U.S.C.
843(a)(3) without some independent determination'' by the respective
state authority. Id. at 4. Respondents thus maintained that
``[d]epriving a practitioner of the right to review of a DEA action
based solely on a State suspension that was in turn based solely on the
original DEA action would violate Due Process.'' Id. at 5. Finally,
Respondents also contended that ``[p]ractitioners may not be able to
obtain review of either suspension, if the State takes the same
position that the [DEA] does here.'' Id.
On June 17, the Government filed its Reply to Opposition to
Government's Motion for Summary Disposition and to Stay the Filing of
Pre-hearing Statements (Reply). The Government argued that ``Indiana
law specifically provides a basis for substantive review of any state
suspension which is triggered by a DEA suspension.'' Reply at 1 (citing
Ind. Code Sec. 35-48-3-5(f)).\2\ The Government further argues that
under DEA precedent, ``when a state suspends a respondent's controlled
substance privileges, Federal revocation is warranted as long as the
respondent has some mechanism to challenge the state action.'' Id. at 2
(citing Odette Louise Campbell, M.D., No. 09-62, Order Remanding for
Further Proceedings).\3\
---------------------------------------------------------------------------
\2\ ``The board may reinstate a registration that has been
suspended under subsection (e), after a hearing, if the board is
satisfied that the applicant is able to manufacture, distribute, or
dispense controlled substances with reasonable skill and safety to
the public.'' Ind. Code Sec. 35-48-3-5(f).
\3\ The Government also argued that ``to the extent that
Respondents argue that the Medical Licensing Board of Indiana * * *
has no authority concerning controlled substance registrations, that
jurisdictional argument must be made to the Board of Pharmacy,'' and
that in ``its letter to [Respondent] Tiwari, the Medical Licensing
Board * * * merely informed Respondent that his CSR was suspended
pursuant to the appropriate statute.'' Reply at 3. Finally, the
Government attached a May 27, 2010 letter from the Indiana Board of
Pharmacy to Respondents which stated that Indiana CSR Number
61100223B, which is held by Respondent PMSC, had been suspended
pursuant to Ind. Code Sec. 35-48-3-5(e). Reply at 3, Ex. 3-A.
---------------------------------------------------------------------------
On June 18, 2010, Respondents filed a Surreply in Opposition to
Government's Motion for Summary Disposition (Surreply), in which they
assert that the Government ``fundamentally misunderstands the Indiana
statutory scheme.'' Surreply, at 1. Therein, the Respondents again
argued that the ``Government's Motion for Summary Disposition should be
denied because it relies on a potential, nonbinding state hearing, a
theoretical possibility that cannot be triggered until the Indiana
Board that actually has authority to suspend the Respondents'
controlled substances registrations issues an order to show cause,
which it has not.'' Id. Respondents further maintained that ``the
Indiana Advisory Committee could avoid the hearing provision on which
the Government relies solely by not issuing the show cause notice.''
Id. at 2.
On June 21, 2010, the ALJ issued an Order for Government's Response
to Surreply in Opposition to Government's Motion for Summary
Disposition. On July 2, 2010, the Government filed its Response to
Surreply. The Government reiterated that the Respondents' Indiana CSRs
have been suspended and that while the issuance of the DEA Immediate
Suspension Orders ``may have been the cause of the state suspension,
[they] do not govern whether those state suspensions remain in
effect.'' Response to Surreply, at 1.
The Government again argued that under Indiana law, the Board of
Pharmacy `` `may reinstate a [CSR] that has been suspended under
subsection (e), after a hearing, if the board is satisfied that the
applicant is able to * * * dispense controlled substances with
reasonable skill and safety to the public.' '' Id. (quoting Ind. Code
Sec. 35-48-3-5(f)). The Government also noted that Respondents had
filed a Petition for Review of the state suspensions, albeit with the
Medical Licensing Board and not the Board of Pharmacy. Id. The
Government argued that this nonetheless demonstrated that Respondents
knew of, and were pursuing, their right to seek administrative review
of the State's suspensions, pursuant to section 35-48-3-5(f).
Next, the Government argued that Respondents' contention that
Indiana must issue an Order to Show Cause prior to suspending their
CSRs is without merit, and that in any case, the issue is a matter of
state law, and not a matter for a DEA ALJ to decide. Response to
Surreply, at 2. Finally, the Government argued that the Respondents'
interpretation of the Indiana statutes would render them inconsistent
and meaningless. Id. at 2-3.
On July 7, 2010, the ALJ issued her recommended decision
(hereinafter ALJ). Therein, the ALJ specifically found that the Indiana
Board of Pharmacy had automatically suspended the Indiana CSRs held by
the Respondents. ALJ at 5. Noting the settled Agency rule that
``possessing authority under state law to handle controlled substances
is an essential condition for holding a DEA registration,'' id. at 6
(quoting Joseph Baumstarck, M. D., 74 FR 17525, 17527 (2009)), and
rejecting Respondents' contention that granting summary disposition
would deny them their right to Due Process, the ALJ granted the
Government's Motion for Summary Disposition. ALJ at 5-7, 9. The ALJ
thus recommended that I revoke the Respondents' DEA Certificates of
Registration and deny any pending applications to renew their
registrations. Id. at 9.
Neither party filed exceptions to the ALJ's decision. Thereafter,
the record was forwarded to me for final agency action.
[[Page 71606]]
Having considered the record as a whole including the parties'
pleadings, I adopt the ALJ's findings of fact and recommended sanction.
I will therefore revoke Respondents' respective DEA Certificates of
Registration and deny any pending applications to renew their
registrations. I make the following findings.
Findings
Respondent Tiwari is the holder of Certificate of Registration
BT2936411, which authorizes him to dispense controlled substances in
schedules II through V, as a practitioner. While this registration was
due to expire on November 30, 2009, on October 2, 2009, Respondent
Tiwari submitted a timely renewal application. Respondent Tiwari's
registration thus remains active, albeit in suspended status, pending
the issuance of the Final Order in this matter. 5 U.S.C. 558(c).
Respondent PMSC is the holder of Certificate of Registration
BP4917413, which authorizes it to dispense controlled substances in
schedules II through V, as a hospital/clinic. This registration is due
to expire on March 31, 2011. According to the registration records of
this Agency, Respondent Tiwari has also submitted an application to
renew Respondent PMSC's registration.
On or about May 27, 2010, the Indiana Board of Pharmacy placed
Respondent PMSC's Indiana CSR in suspended status. See Reply to Opp. to
Gov. Mot. for Summ. Disp., at Ex. 3-A. Moreover, according to a letter
from the MLB to Respondent Tiwari, on or about May 26, 2010, his
Indiana CSR was placed in suspended status. Id. at Ex. 3. According to
the Indiana Online Licensing Web site, of which I take official notice,
each Respondent's CSR remains suspended as of the date of this Decision
and Final Order.\4\
---------------------------------------------------------------------------
\4\ Under the Administrative Procedure Act (APA), an agency
``may take official notice of facts at any stage in a proceeding-
even in the final decision.'' U.S. Dept. of Justice, Attorney
General's Manual on the Administrative Procedure Act 80 (1947) (Wm.
W. Gaunt & Sons, Inc., Reprint 1979). In accordance with the APA and
DEA's regulations, Respondent is ``entitled on timely request, to an
opportunity to show to the contrary.'' 5 U.S.C. 556(e); see also 21
CFR 1316.59(e). Respondent can dispute the facts of which I take
official notice by filing a properly supported motion for
reconsideration within twenty days of service of this Order, which
shall begin on the date it is mailed.
---------------------------------------------------------------------------
Discussion
Under the Controlled Substances Act (CSA), a practitioner must be
currently authorized to handle controlled substances in ``the
jurisdiction in which he practices'' in order to maintain a DEA
registration. See 21 U.S.C. 802(21) (``[t]he term `practitioner' means
a physician * * * pharmacy, hospital, 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''). See
also id. Sec. 823(f) (``The Attorney General shall register
practitioners * * * if the applicant is authorized to dispense * * *
controlled substances under the laws of the State in which he
practices.''). As these provisions make plain, possessing authority
under state law to handle controlled substances is an essential
condition for obtaining and maintaining a practitioner's registration.
Accordingly, DEA has held that revocation of a practitioner's
registration is warranted whenever his (or its) state authority to
dispense controlled substances has been suspended or revoked. David W.
Wang, 72 FR 54297, 54298 (2007); Sheran Arden Yeates, 71 FR 39130,
39131 (2006); Dominick A. Ricci, 58 FR 51104, 51105 (1993); Bobby
Watts, 53 FR 11919, 11920 (1988). See also 21 U.S.C. 824(a)(3)
(authorizing revocation of a registration ``upon a finding that the
registrant * * * has had his State license or registration suspended
[or] revoked * * * and is no longer authorized by State law to engage
in the * * * distribution [or] dispensing of controlled substances'').
DEA has further held that revocation is warranted even where a
practitioner's state authority has been summarily suspended and the
State has yet to provide the practitioner with a hearing to challenge
the State's action and at which he (or it) may ultimately prevail. See
Robert Wayne Mosier, 75 FR 49950 (2010) (``revocation is warranted * *
* even in those instances where a practitioner's state license has only
been suspended, and there is the possibility of reinstatement'');
accord Bourne Pharmacy, 72 FR 18273, 18274 (2007); Anne Lazar Thorn, 62
FR 12847 (1997).
Here, it is undisputed that the State has suspended the state
controlled substance registration of each Respondent. DEA has long held
that the order of a state agency suspending or revoking a
practitioner's state authority cannot be collaterally attacked in a
proceeding under the CSA. See Hicham K. Riba, 73 FR 75773, 75774 (2008)
(rejecting claim that state proceeding was fundamentally unfair based
on alleged improper ex parte influence of director of state board as
``not addressable in'' DEA proceeding); Sunil Bhasin, 72 FR at 5082,
5083 (2007) (rejecting claim that settlement agreement in which
Respondent surrendered state license was produced by fraud and was
unconscionable; ``a DEA Show Cause Proceeding is not the proper forum
to litigate the issue''); see also Shahid Musud Siddiqui, 61 FR 14818
(1996); Robert A. Leslie, 60 FR 14004 (1995).
The underlying premise of these cases is that the States exercise
sovereign powers in regulating the medical profession and that
challenges to the validity of state board orders should be raised and
litigated in state forums. See, e.g., Riba, 73 FR at 75774 (claim that
``state proceeding was fundamentally unfair * * * is not addressable
in'' DEA proceeding). These cases likewise implicitly recognize that
state boards and state courts are fully cognizant of their obligation
under the Due Process Clause to provide a full and fair opportunity to
litigate the issues. Cf. University of Tennessee v. Elliott, 478 U.S.
788, 797-98 (1986) (``When an administrative agency is acting in a
judicial capacity and resolves disputed issues of fact properly before
it which the parties have had an adequate opportunity to litigate, the
courts have not hesitated to apply res judicata[.]'') (int. quotations
and citations omitted).
It is true that in Odette Louise Campbell, M.D., No. 09-62, I
denied the Government's request for a final order based on the
registrant's loss of her controlled substance prescribing authority
under Texas law where the State had suspended that authority based on
DEA's issuance of an immediate suspension order and remanded the matter
for further proceedings. Campbell, Order Remanding for Further
Proceedings, at 10-11. However, I noted that specific provisions of
Texas law and regulations suggested that the registrant was not
entitled to a hearing to challenge the merits of the state suspension
because it was based on the DEA immediate suspension. Id. at 9 (citing
Texas Health & Safety Code Sec. Sec. 481.063(e)(3), 481.063(h),
481.066(g), and Tex. Admin. Code Sec. 13.272(h)). Moreover, I ordered
the ALJ to first determine whether the State had provided, or would
provide, the registrant with a hearing; I further ordered that if the
State had provided or would provide a hearing, the Government could
renew its motion for summary disposition. Id. at 10.
By contrast, while the Indiana Board(s) suspended Respondents'
state registrations based on the state law provision that ``[i]f the
Drug Enforcement Administration * * * suspends * * * a federal
registration for the * * * dispensing of controlled substances, a
registration issued by the board under this chapter is automatically
suspended,'' Ind. Code
[[Page 71607]]
Sec. 35-48-3-5(e), state law further provides that ``[t]he board may
reinstate a registration that has been suspended under subsection(e)
after a hearing, if the board is satisfied that the applicant is able
to manufacture, distribute or dispense controlled substances with
reasonable skill and safety to the public.'' Id. Sec. 35-48-3-5(f).
(emphasis added). Thus, it appears that Respondents are entitled to a
hearing to challenge the underlying allegations before the State board.
Respondents contend that their right to a hearing under section 35-
48-3-5(f) ``is not triggered until the Indiana Controlled Substances
Advisory Committee serves upon the * * * registrant an order to show
cause why registration should not be denied, revoked or suspended,''
and that ``absent such a step, the purported suspension issued by the
board * * * is a nullity, and cannot form the basis for a federal
suspension.'' Surreply at 2 (citing Ind. Code Sec. 35-48-3-6(a)).\5\
Respondents further argue that ``[i]f it could, then the Indiana
Advisory Committee could avoid the hearing provision on which the
Government relies solely by not issuing the show cause notice.'' Id.
---------------------------------------------------------------------------
\5\ This provision states:
Before recommending a denial, suspension, or revocation of a
registration, or before refusing a renewal of registration, the
board shall serve upon the applicant or registrant an order to show
cause why registration should not be denied, revoked, or suspended *
* *. The order to show cause shall contain a statement of the basis
therefor [sic] and shall call upon the applicant or registrant to
appear before the board at a time and place not less than thirty
(30) days after the date of service of the order * * *.
---------------------------------------------------------------------------
Beyond the fact that Respondents' argument appears to be based on
the speculative premise that the Indiana authorities will attempt to
prevent them from obtaining a hearing, the Indiana statute makes clear
that Respondents are entitled to a hearing. Presumably, the Indiana
courts are open and can provide an appropriate remedy in the event the
state board refuses to provide Respondents with a hearing. See Ind.
Code Sec. 34-27-3-1 (``An action for mandate may be prosecuted against
any inferior tribunal * * * public * * * officer, or person to compel
the performance of any * * * act that the law specifically
requires[.]'').
Moreover, the question of whether the Indiana suspensions are a
nullity because the State did not serve Respondents with a Show Cause
Order is an issue of state law and for the Indiana courts to decide. As
such, it is outside the scope of this proceeding. See George S. Heath,
M.D., 51 FR 26610 (1986) (``DEA accepts as valid and lawful the action
of a state regulatory board unless that action is overturned by a state
court or otherwise pursuant to state law. * * * The [DEA] will not
consider a challenge to the lawfulness of a Georgia Board Order. Such a
challenge must be made in another forum.''); see also Shahid Musud
Siddiqui, M.D., 61 FR 14818, 14818-19 (DEA 1996) (A ``DEA
administrative proceeding is not an appropriate forum for wholesale
review of state criminal and administrative actions taken by the State
of New York arising out of the laws of the State of New York. To allow
it to be so would be to permit a wide collateral attack upon such
convictions.'') (int. quotations and citation omitted).
Finally, Respondents argue that the suspensions of their state CSRs
are invalid because they were suspended by the MLB and only the
Pharmacy Board has authority under state law to suspend their
registrations. However, the Pharmacy Board's May 27, 2010 letter makes
clear that it (and not the MLB) was suspending Respondent PMSC's
registration, and even if Respondent Tiwari's controlled substance
registration was suspended by the MLB, the validity of this action is
also a question of state law and for the Indiana courts to decide.
Riba, 73 FR at 75774; Heath, 51 FR at 26610.
Because there is no dispute over the material fact that each
Respondent's Indiana controlled substance registration has been
suspended, each is without authority to hold a DEA registration.\6\ See
21 U.S.C. 802(21). Accordingly, Respondents' registrations will be
revoked and any pending applications will be denied.
---------------------------------------------------------------------------
\6\ Where, as here, no material fact is in dispute, there is no
need for an evidentiary hearing and summary disposition is
appropriate. See Michael G. Dolin, M.D., 65 FR 5661 (2000); see also
Philip E. Kirk, M.D., 48 FR 32887 (1983), aff'd sub nom Kirk v.
Mullen, 749 F.2d 297 (6th Cir. 1984).
---------------------------------------------------------------------------
Order
Pursuant to the authority vested in me by 21 U.S.C. 823(f) and
824(a), as well as 28 CFR 0.100(b) and 0.104, I order that DEA
Certificate of Registration, BT2936411, issued to Respondent Kamal
Tiwari, M.D., and DEA Certificate of Registration, BP4917413, issued to
Respondent Pain Management and Surgery Center of Southern Indiana, be,
and they hereby are, revoked. I further order that any pending
applications of Kamal Tiwari, M.D. and Pain Management and Surgery
Center of Southern Indiana, to renew or modify such registrations, be,
and they hereby are, denied. This Order is effective immediately.\7\
---------------------------------------------------------------------------
\7\ For the same reason that I ordered that the Respondents'
registration be immediately suspended, I conclude that the public
interest necessitates that this Order be effective immediately. See
21 CFR 1316.67.
Dated: November 8, 2011.
Michele M. Leonhart,
Administrator.
[FR Doc. 2011-29708 Filed 11-17-11; 8:45 am]
BILLING CODE 4410-09-P