Rick's Picks, L.L.C.; Revocation of Registration, 18275-18280 [E7-6759]
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Examiners. Under the order,
Respondent’s Texas medical license was
revoked.
Thereafter, on July 13, 2006, the ALJ
denied Respondent’s request to stay the
hearing until after his release from
prison. ALJ Dec. at 2. The ALJ further
ordered that Respondent file a response
to the Government’s motion by August
3, 2006. Respondent, however, failed to
do so.
Thereafter, the ALJ granted the
Government’s motion. The ALJ noted
that Respondent ‘‘acknowledges that his
license to practice medicine in Texas is
revoked, and will remain revoked at
least until his release from prison on
April 7, 2007.’’ Id. As this material fact
was undisputed, the ALJ held that
because ‘‘Respondent lacks state
authority, he is not entitled to a DEA
registration in Texas,’’ and therefore
recommended that Respondent’s
registration be revoked. Id. at 2–3. The
ALJ then forwarded the record to me for
final agency action.
Having considered the record as a
whole, I adopt the ALJ’s
recommendation that Respondent’s
registration be revoked. But in doing so,
I decline to adopt the ALJ’s reasoning to
the extent it relies solely on the Texas
State Board of Medical Examiner’s
revocation of Respondent’s medical
license. Under Texas law, a practitioner
must obtain a separate state registration
to dispense a controlled substance.
Texas Health & Safety Code § 481.061.
The record, however, contains no
evidence regarding the status of
Respondent’s state registration.
Therefore, in accordance with 5
U.S.C. 556(e), I take official notice of the
fact that according to the Texas
Department of Public Safety’s
Controlled Substances Registration
verification search page, Respondent is
not currently registered to dispense
controlled substances in the State.1
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 * * * licensed, registered, or
otherwise permitted, by * * * the
jurisdiction in which he practices * * *
to distribute, dispense, [or] administer
1 Under the Administrative Procedure Act,
‘‘[a]gencies may take official notice of facts at any
stage in a proceeding—even in the final decision.’’
Attorney General’s Manual on the Administrative
Procedure Act 80 (1946) ( Wm. W. Gaunt & Sons,
Inc., reprint 1979). In accordance with the Act,
Respondent may ‘‘show to the contrary’’ by filing
a request for reconsideration which includes
supporting documentation within fifteen days of
receipt of this order.
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* * * a controlled substance in the
course of professional practice’’). See
also id. section 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.’’). DEA has held repeatedly
that the CSA requires the revocation of
a registration issued to a practitioner
who no longer possesses authority
under state law to handle controlled
substances. See 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 the
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’’). Therefore,
Respondent’s DEA registration must be
revoked.2
Order
Accordingly, pursuant to the
authority vested in me by 21 U.S.C.
823(f) & 824(a), as well as 28 CFR
0.100(b) & 0.104, I hereby order that
DEA Certificate of Registration,
AP1614800, issued to Piyush V. Patel,
M.D., be, and it hereby is, revoked. I
further order that any pending
applications for renewal or modification
of such registration be, and they hereby
are, denied. This order is effective May
11, 2007.
Dated: March 30, 2007.
Michele M. Leonhart,
Deputy Administrator.
[FR Doc. E7–6761 Filed 4–10–07; 8:45 am]
BILLING CODE 4410–09–P
DEPARTMENT OF JUSTICE
Drug Enforcement Administration
[Docket No. 05–8]
Rick’s Picks, L.L.C.; Revocation of
Registration
On October 7, 2004, the Deputy
Assistant Administrator, Office of
Diversion Control, Drug Enforcement
Administration, issued an Order to
Show Cause to Rick’s Picks, L.L.C.
(Respondent), of Moore, Oklahoma. The
Show Cause Order proposed the
revocation of Respondent’s DEA
Certificate of Registration, 003949RPY,
as a distributor of list I chemicals, on
the ground that its continued
2 The expiration date of Respondent’s DEA
registration is March 31, 2008.
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registration was inconsistent with the
public interest. Show Cause Order at 1
(citing 21 U.S.C. 823(h)).
The Show Cause Order incorporated
the allegations of a show cause order
which was initiated by the Oklahoma
State Bureau of Narcotics and
Dangerous Drugs Control; the latter
order proposed the denial of
Respondent’s application for a state
registration to distribute
pseudoephedrine products that are
Schedule V drugs under State law, as
well as the revocation of Respondent’s
state registration to distribute
pseudoephedrine products which are
not scheduled under state law. Id. at 2.
Specifically, the state show cause order
alleged that Respondent and its owner,
Rick D. Fowler, ‘‘have a history of
selling very large amounts of
pseudoephedrine under suspicious and
questionable circumstances, and with
great negligence and reckless disregard
for whether this product would be used
in the clandestine manufacture of
methamphetamine,’’ and that
Respondent, and its owner, had engaged
in this activity notwithstanding
‘‘numerous warnings from . . . DEA
officials that Respondent’s sales were
fueling illicit methamphetamine
laboratories.’’ Id.
Relatedly, the State show cause order
alleged that from January 2002 through
April 2004, Respondent sold more than
$ 2.2 million of Max Brand (for a total
of nearly 10.5 million tablets), a product
in which pseudoephedrine is the single
active ingredient and which is the
‘‘preferred choice [of]
methamphetamine cooks.’’ Id. at 4–5.
The state show cause order also alleged
that Respondent had brokered the sale
of approximately 400,000
pseudoephedrine tablets for D & E
Pharmaceutical. Id. at 5. The DEA Show
Cause Order then repeated ten different
allegations made in the state show cause
order which asserted specific instances
in which Respondent had sold
extraordinary quantities of
pseudoephedrine to convenience stores,
gas stations and other non-traditional
retailers of this product, and that
Respondent had failed to report any of
these transactions to DEA. Id. at 6–8.
The State show cause order further
alleged that pseudoephedrine
distributed by Respondent had been
found at twenty-two methamphetamine
dumpsites. Id. at 8. Finally, the DEA
Show Cause Order alleged that in
November 2003, DEA had conducted an
inspection of Respondent during which
numerous recordkeeping violations
were observed. Id. at 9.
Respondent requested a hearing on
the allegations. The matter was assigned
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to Administrative Law Judge (ALJ) Mary
Ellen Bittner, who conducted a hearing
in Oklahoma City, Oklahoma, on
January 10 and 11, 2006. At the hearing,
the Government introduced both
testimonial and documentary evidence;
Respondent introduced only
documentary evidence. Both parties
submitted post-hearing briefs.
On August 9, 2006, the ALJ issued her
decision. In that decision, the ALJ
concluded that Respondent’s continued
registration would be inconsistent with
the public interest and recommended
that its registration be revoked. Neither
party filed exceptions.
Having considered the record as a
whole, I hereby issue this decision and
final order. I adopt the ALJ’s findings of
fact and conclusions of law in their
entirety. For the reasons set forth below,
I hold that Respondent’s continued
registration would be inconsistent with
the public interest and therefore revoke
its registration and deny its pending
application for renewal.
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Findings
Respondent, an Oklahoma
corporation, is a distributor of assorted
merchandise to convenience stores, gas
stations, and other small retailers in that
State. Respondent’s sole owner is Mr.
Rickey Fowler. ALJ Dec. at 15.
Respondent currently holds DEA
Certificate of Registration, 003949RPY,
which authorizes it to distribute list I
chemicals. Gov. Ex. 1. While
Respondent’s registration certificate
states that its registration expired on
April 30, 2005, the record indicates that
Respondent filed a timely renewal
application. Tr. 24. Therefore,
Respondent’s registration remains in
effect until the conclusion of this
proceeding. See 5 U.S.C. 558(c).
Methamphetamine and the Market for
List I Chemicals
Pseudoephedrine is lawfully
marketed under the federal Food, Drug
and Cosmetic Act for over-the-counter
use as a decongestant. Pseudoephedrine
is, however, also regulated as a list I
chemical under the Controlled
Substances Act because it is easily
extracted from non-prescription
products and used in the illicit
manufacture of methamphetamine, a
Schedule II controlled substance. See 21
U.S.C. 802(34); 21 CFR 1308.12(d).
Methamphetamine ‘‘is a powerful and
addictive central nervous system
stimulant.’’ T. Young Associates, Inc.,
71 FR 60567 (2006). The illegal
manufacture and abuse of
methamphetamine pose a grave threat to
this country. Methamphetamine abuse
has destroyed numerous lives and
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families and ravaged communities.
Moreover, because of the toxicity of the
chemicals used in producing the drug,
its illicit manufacture causes serious
environmental harms. Id.
Methamphetamine abuse has been an
especially serious problem in the State
of Oklahoma. In 1999, law enforcement
authorities seized 391 illicit
laboratories/dumpsites in the State; in
2003 (the last full year before the State
enacted laws restricting the distribution
of pseudoephedrine), authorities seized
1091 illicit laboratories/dumpsites. See
Gov. Exs. 7 & 11. Moreover, in 2004,
there were still 659 seizures. See Gov.
Ex. 12. According to a senior agent for
the Oklahoma Bureau of Narcotics, Max
Brand in tablet form, a product in which
pseudoephedrine (60 mg.) is the single
active ingredient, is the preferred
product of the State’s illicit
methamphetamine cooks.1 See also Tr.
46 & 180.
In the course of adjudicating
numerous cases, DEA has acquired
substantial expertise pertaining to the
market for list I chemical products
containing pseudoephedrine.
Accordingly, pursuant to 5 U.S.C.
556(e), I take official notice of the
following facts related to the market for
pseudoephedrine.2
According to Jonathan Robbin, an
expert in statistical analysis of
demographic, economic, geographic and
survey data, ‘‘over 97% of all sales of
non-prescription drug products occur in
drug stores and pharmacies,
supermarkets, large discount
merchandisers and electronic shopping
and mail order houses.’’ T. Young, 71
FR at 60568. Moreover, ‘‘sales of nonprescription drugs by convenience
stores (including both those that sell
and do not sell gasoline), account for
only 2.2% of the overall sales of all
convenience stores that handle the line
and only 0.7% of the total sales of all
convenience stores.’’ Id.
Based on his study of U.S.
Government Economic Census Data,
1 In response to the methamphetamine problem,
effective April 6, 2004, Oklahoma made
pseudoephedrine in tablet form a Schedule V
controlled substance. Pseudoephedrine in liquid,
liquid-filled capsules, and gel caps is, however,
exempt from the requirement provided it is not the
only active ingredient in the product. See 63 Okl.
St. Ann. section 2–212.
2 Under the Administrative Procedure Act,
‘‘[a]gencies may take official notice of facts at any
stage in a proceeding-even in the final decision.’’
Attorney General’s Manual on the Administrative
Procedure Act 80 (1946) ( Wm. W. Gaunt & Sons,
Inc., reprint 1979). In accordance with the Act,
Respondent may request a reopening of the
proceeding to contest the facts of which I am taking
official notice by filing a request with supporting
affidavits no later than fifteen days after service of
this order.
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information obtained from the National
Association of Convenience Stores, and
commercially available point of sale
transaction data, Mr. Robbin has
constructed a model of the traditional
market for retail sales of
pseudoephedrine. See id. According to
Mr. Robbin, ‘‘sales of pseudoephedrine
account for only about 2.6% of the sales
of health and beauty care products in
convenience stores and only 0.05% of
total in-store (non-gasoline) sales.’’ Id.
Moreover, ‘‘the normal expected retail
sale of pseudoephedrine (Hcl) tablets in
a convenience store may range between
$ 0 and $ 40 per month, with an average
of $ 20.60 per month.’’ Id. According to
Mr. Robbin, a monthly retail sale at a
non-traditional retailer of ‘‘$ 60 of
pseudoephedrine would occur less than
one in 1,000 times in random
sampling.’’ Id. Moreover, a monthly
retail sale of ‘‘$ 100 in pseudoephedrine
would occur about once in a million
times in random sampling.’’ Id.
Findings Pertaining To Respondent
Respondent first became registered to
distribute list I chemicals in January
1999. Prior to becoming registered, DEA
Diversion Investigators (DIs) conducted
a pre-registration investigation. During
this visit, the DIs discussed with Mr.
Fowler the recordkeeping requirements
imposed by federal law and regulations.
Tr. 32–33. The DIs also provided Mr.
Fowler with DEA notices that discussed
suspicious transactions and advised that
certain list I chemical products
including pseudoephedrine were being
diverted into the illicit manufacture of
methamphetamine. Id. at 34. One of the
notices specifically stated that ‘‘[t]he
exemption from certain recordkeeping
and reporting requirements for below
threshold transactions . . . does not
reduce the risk of criminal liability.’’
Gov. Ex. 3. This notice also advised Mr.
Fowler to ‘‘[r]eport all suspicious orders
to your nearest DEA office
immediately.’’ Id.
The DIs, however, also gave Mr.
Fowler a handout listing required
reports. See Resp. Ex. 18, Tr. 64. More
specifically, this document stated that
reports were required for ‘‘[a]ny
regulated transaction involving an
extraordinary quantity of a Listed
Chemical,’’ ‘‘[a]ny regulated transaction
involving an uncommon method of
payment or delivery,’’ and ‘‘[a]ny
regulated transaction involving any
other circumstances that the regulated
person (supplier) believes may indicate
that the List (sic) Chemical will be used
in the illicit production of controlled
substances.’’ Resp. Ex. 18.
In September 2001, DEA DIs returned
to Respondent for a scheduled
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inspection. Among other things, the DIs
determined that Respondent was storing
list I chemicals in a trailer at a boat
storage and not at its registered location.
Id. at 37. The DIs also found that
Respondent was in violation of
recordkeeping requirements because its
receiving invoices did not include the
date that products were received and its
sales invoices did not indicate package
size. Id. at 38. Respondent’s owner was
issued a letter admonishing him for the
violations. Resp. Ex. 2. Subsequently,
Mr. Fowler wrote to one of the DIs
advising of changes Respondent would
make in its recordkeeping; at that time,
DEA took no further action. ALJ Dec. at
16.
On November 3, 2003, DEA DIs
conducted another inspection of
Respondent. The DIs determined that
while Respondent was now properly
storing its list I chemical products, it
was still violating the recordkeeping
requirements. See id. at 16–17. DEA
issued Respondent an additional letter
of admonition. Tr. 41. During this visit,
DEA also obtained Respondent’s
receiving and sales invoices for the
period from January 1, 2002, through
November 1, 2003. Id. at 261; Resp. Ex.
25.3
In May 2004, law enforcement
authorities obtained a warrant and
executed a search of Respondent. Based
on records obtained during the search,
as well as the records obtained during
the November 2003 inspection, DEA
investigators compiled a spreadsheet of
Respondent’s purchases of
pseudoephedrine. Gov. Ex. 21; Tr. 187.
According to this document, between
January 28, 2002, and March 6, 2004,
Respondent had purchased 10,062,144
tablets of Max Brand pseudoephedrine
at a wholesale price of $ 941,072.20. Id.
Moreover, during the 2003 calendar
year, Respondent purchased nearly six
million tablets at a wholesale price of $
564,884.20. Id. Furthermore, between
January 5, 2004, and March 6, 2004
(shortly before the Oklahoma statute
scheduling tablet-form pseudoephedrine
became effective), Respondent
purchased approximately 1.8 million
tablets at a wholesale price of $ 173,004.
Id.
DEA investigators also compiled a
spreadsheet of Respondent’s
pseudoephedrine sales. See Gov. Ex. 23.
This 102 page document lists
Respondent’s sales to each store by
product size and date. The document
shows that Respondent repeatedly made
3 On April 7, 2004, a DEA DI again returned to
Respondent to discuss the then-recently enacted
state legislation which scheduled pseudoephedrine
in tablet form. During this visit, the DI conducted
a closing inventory. ALJ Dec. at 17.
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monthly sales of a $ 1,000 or more of
pseudoephedrine products to the great
majority of the stores.4 See generally id.
For example, from January 2002
through April 6, 2004, Respondent sold
$ 62,658.00 (and brokered the sale of $
7,013) of pseudoephedrine to
Bernhardt’s, a convenience store in
Pharoah, Oklahoma. Gov. Ex. 24, at 5.
During the same period, Respondent
sold $ 50,256 (and brokered the sale of
$ 7,015) of pseudoephedrine to Dock’s
General Store in Council Hill,
Oklahoma, and sold $ 44,640 (and
brokered the sale of $ 7,015) of the
chemical to Dock’s General Store in
Leonard, Oklahoma. Id. at 6–7. Both of
these establishments were bait and
tackle shops. Tr. 269–71. Respondent
also sold $ 37,116 (and brokered the sale
of $ 4,676) of the chemical to Kern’s
Korner Grocery in Henryetta, Oklahoma.
Gov. Ex. 24, at 8. Furthermore, from
January 2002 through December 2002,
Respondent sold $ 11,880 of
pseudoephedrine to the Funky Munky,
a head shop located in McAlester,
Oklahoma. Id. at 9; see also Tr. 273.
The record also establishes that
between February 2002 and March
2004, Respondent sold $ 97,026 (and
468,144 tablets) of pseudoephedrine to
five stores in Poteau, a small city in
eastern Oklahoma. Of significance
among these customers, Respondent
sold $ 30,672 to Babe’s Place and $
37,590 to the Tote-A-Poke # 1. Gov. Ex.
24, at 3. It also sold $14,040 to Burkes
Friendly Store; all of the sales to Burkes
occurred between February 2002 and
March 2003. Gov. Ex. 23, at 15–16.
The above per-store figures are based
on Respondent’s wholesale prices.
Several of Respondent’s exhibits
indicate that the suggested retail price
was typically twice the wholesale price.
See Resp. Exh. 20, at 19; Resp. Ex. 19.
Ultimately, even if Respondent’s
customers sold the products at far less
than the suggested retail prices, their
sales of these products so greatly
exceeded the monthly expected sales
range of $ 0 to $ 40, with an average of
$ 20.60, that the probability that the
products were being purchased to meet
legitimate consumer demand for use as
a decongestant is infinitesimal. Indeed,
as DEA’s expert has testified, a monthly
retail sale of $ 100 in pseudoephedrine
to meet legitimate demand would occur
about once in a million times in random
4 One of the DIs testified that her review of
Respondent’s records showed that its sales of
pseudoephedrine constituted eighty-five percent of
its business. ALJ Dec. at 17. The Government also
introduced evidence that Respondent brokered the
sale of substantial amounts of ‘‘Bolt’’ brand
pseudoephedrine directly from its manufacturer to
various stores. Tr. 273–276; Gov. Ex. 24, at 5–8.
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sampling. Here, where there are
numerous stores to which Respondent
sold repeatedly $ 1,000 or more per
month at wholesale prices, the only
plausible explanation is that the
products were being diverted into the
illicit manufacture of
methamphetamine.5 I thus find that
substantially all of Respondent’s
products were being diverted.
The ALJ further credited the
testimony of a DEA investigator that
‘‘some of Respondent’s customers
engaged in practices that the DEA
considers suspicious.’’ ALJ at 18. More
specifically, these practices included:
(1) Ordering only single-entity
pseudoephedrine rather than a variety
of pseudoephedrine and other over-thecounter drug products, (2) selling singleentity products that are marketed in
large quantities and not in blister packs,
(3) selling products that have only been
on the market for a few years and which
receive little advertising, and (4)
purchasing large quantities of
pseudoephedrine throughout the year
by establishments that traditionally do
not sell large quantities of these
products and do little or no marketing
of them.6 ALJ at 18, Tr. 349–51.
The ALJ further found that
‘‘Respondent never sold more than the
[1000 grams] threshold amount to any
one customer in a calendar month.’’ ALJ
at 20. The ALJ also found that
Respondent’s owner twice ‘‘reported a
suspicious sale to’’ DEA. Id. According
to the record, on October 8, 2003, Mr.
Fowler reported that while servicing a
store the previous day, ‘‘the store clerk
made a comment that she needed
products that Methamphetamine is
made from.’’ Resp. Ex. 6, at p. 2. Mr.
Fowler further wrote that he had
‘‘suspended sales of all pseudo
ephedrine products to this store due to
this comment,’’ and that he would ‘‘not
service this store in the future with any
cold medications containing pseudo
ephedrine.’’ Id. Approximately, a month
5 During cross-examination, Respondent’s counsel
elicited testimony from a Government witness that
a few of the stores it sold to were located on
highways—thus suggesting that the sales at these
stores were to meet legitimate consumer demand.
Tr. 201–02. This testimony does not persuade me
that Respondent’s products were being sold to meet
legitimate demand. The ALJ found that Respondent
had more than 200 customers, see ALJ Dec. at 18;
Respondent’s line of cross-examination begs the
question: What about the other 200 plus stores?
Indeed, the ALJ found that ‘‘some of Respondent’s
customers were convicted of criminal charges
involving the diversion of pseudoephedrine.’’ Id.
6 Most of these indicia were published by DEA in
February 1999. See Suspicious Orders Task Force,
Report to the U.S. Attorney General Appendix A
(1999). The indicia were re-published in the June
2002 Chemical Handler’s Manual. See DEA,
Chemical Handler’s Manual—A Guide to Chemical
Control Regulations 40–43 (June 2002).
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later Mr. Fowler also reported that he
had been contacted by a person who
wanted to come to his premises to
purchase products but Mr. Fowler
advised him that his firm ‘‘did not do
business this way.’’ Id. at 3. Mr. Fowler
further stated that the address given by
this person was non-existent and that he
had determined that the business was
not legitimate.7 Id.
On November 14, 2005, the Cleveland
County, Oklahoma, District Attorney
filed a felony information charging Mr.
Fowler with criminal racketeering under
Oklahoma law. Gov. Ex. 42. More
specifically, the information alleged that
‘‘between January 2002 and April
2004,’’ Fowler ‘‘was willfully,
knowingly and criminally associated
with an enterprise,’’ which consisted of
himself, ‘‘individually, and as the owner
of Rick Picks,’’ the affairs of which
‘‘were to distribute pseudoephedrine, a
precursor in the manufacturing of
methamphetamine, with reckless
disregard for how the product was going
to be used in violation of 63 O.S. 2–
333(A).’’ Id. I further take official notice
of the fact that on October 16, 2006, the
State filed a second amended felony
information charging Respondent with
the ‘‘unlawful distribution of
pseudoephedrine with reckless
disregard for how it was going to be
used.’’ Finally, I take official notice of
the fact that on February 9, 2007, a jury
found Mr. Fowler guilty of the crime
charged in the second amended
information. See Docket Sheet, State v.
Fowler, No. CF–2005–1651, Cleveland
County, Oklahoma, District Court.
Discussion
Section 304(a) of the Controlled
Substances Act provides that a
registration to distribute a list I chemical
‘‘may be suspended or revoked * * *
upon a finding that the registrant * * *
has committed such acts as would
render his registration under section 823
of this title inconsistent with the public
interest as determined under such
section.’’ 21 U.S.C. 824(a)(4). In making
this determination, Congress directed
that I consider the following factors:
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(1) Maintenance by the [registrant] of
effective controls against diversion of listed
chemicals into other than legitimate
channels;
(2) compliance by the applicant with
applicable Federal, State, and local law;
(3) any prior conviction record of the
applicant under Federal or State laws relating
7 While Respondent introduced several form
letters to customers purporting to impose
requirements for the sale of pseudoephedrine, Resp.
Exs. 11–13, as the ALJ noted, ‘‘Respondent did not
call any witnesses at the hearing, and there is no
evidence as to whether such letters were mailed to
Respondent’s customers.’’ ALJ Dec. at 19.
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to controlled substances or to chemicals
controlled under Federal or State law;
(4) any past experience of the applicant in
the manufacture and distribution of
chemicals; and
(5) such other factors as are relevant to and
consistent with the public health and safety.
further steps to determine the ultimate
disposition of his products.
Respondent’s understanding is
mistaken. Congress’s imposition of
recordkeeping and reporting
requirements for regulated transactions
does not mean that one can engage in
Id. section 823(h).
below-threshold transactions without
‘‘These factors are considered in the
any further obligation to determine
disjunctive.’’ Joy’s Ideas, 70 FR 33195,
whether the products are likely to be
33197 (2005). I may rely on any one or
diverted. Indeed, DEA has found that
a combination of factors, and may give
products which have been distributed to
each factor the weight I deem
non-traditional retailers in subappropriate in determining whether a
threshold transactions are routinely
registration should be revoked or an
diverted. Contrary to Respondent’s
application for renewal of a registration
view, the threshold provisions
should be denied. See, e.g., David M.
pertaining to regulated transactions do
Starr, 71 FR 39367, 39368 (2006);
not create a safe harbor which allows a
Energy Outlet, 64 FR 14269 (1999).
registrant to sell list I chemicals without
Moreover, I am ‘‘not required to make
any further duty to investigate how the
findings as to all of the factors.’’ Hoxie
products are being used.
v. DEA, 419 F.3d 477, 482 (6th Cir.
Respondent further contends that
2005); Morall v. DEA, 412 F.3d 165,
‘‘[t]here was no evidence presented that
173–74 (D.C. Cir. 2005). In this case, I
[it] had actual knowledge [that] any
hold that factors one, two, four, and five customer was diverting
overwhelmingly establish that
pseudoephedrine for the manufacture of
Respondent’s continued registration
methamphetamine.’’ Id. at 10. In short,
would be ‘‘inconsistent with the public
Respondent raises the ostrich defense.
interest.’’ 21 U.S.C. 823(h). Accordingly,
Congress, however, has rejected the
I further hold that Respondent’s
ostrich defense in creating criminal
registration should be revoked and its
liability under 21 U.S.C. 841(c)(2), and
pending application for renewal should I have previously rejected this defense
as incompatible with the purpose of
be denied.
proceedings under 21 U.S.C. 823 and
Factor One—Maintenance of Effective
824, which are brought to protect the
Controls Against Diversion
public interest. See D & S Sales, 71 FR
I concur with the ALJ’s conclusion
at 37612; T. Young Associates, 71 FR at
that the record does not establish that
60572. As D & S Sales explained:
Respondent fails to provide adequate
‘‘Burying one’s head in the sand while
physical security for list I chemicals.
his firm’s products are being diverted
However, ‘‘’[p]rior agency rulings have
may allow one to maximize profits. But
applied a more expansive view of factor it is manifestly inconsistent with public
one than mere physical security.’’ ’ D &
health and safety.’’ 71 FR at 37612.
S Sales, 71 FR 37607, 37610 (2006)
More recently, I revoked a registration
(quoting OTC Distribution Co., 68 FR
holding—albeit in the context of
70538, 70542 (2003)). Relatedly, I have
analyzing factors four and five—that a
previously held that a registrant is
registrant’s lack of ‘‘any intent to divert
‘‘required to exercise a high degree of
or to sell to customers who were
care in monitoring its customers’
diverting to the illicit manufacture of
purchases.’’ D & S Sales, 71 FR at 37610. methamphetamine is irrelevant.’’ T.
Respondent argues that he maintains
Young, 71 FR at 60572. See also Joy’s
effective controls against diversion
Ideas, 70 FR at 33198 (revoking
because he obtained proof of identity
registration notwithstanding that
from his customers and only distributed distributor was ‘‘an unknowing and
to ‘‘legitimate store[s],’’ Resp. Statement unintentional contributor to [the]
of Supporting Reasons 9 [hereinafter
methamphetamine problem.’’).
Respondent’s owner also contends
Resp. Br.], he maintained adequate and
that he maintained adequate controls
retrievable records, id., and he ‘‘did not
fail to report suspicious sales because he because he ‘‘reported suspicious
activities to the DEA in the past.’’ Resp.
was only required to report suspicious
Br. at 9. According to the record, Mr.
regulated transactions,’’ i.e.,
Fowler reported an encounter he had
transactions that exceeded the 1,000
during which a store clerk informed him
grams threshold. Id. at 11 (citing 21
‘‘that she needed products that
U.S.C. 830(b)(1) and 21 CFR
Methamphetamine is made from.’’ Resp.
1310.05(a)(1)).
Respondent apparently believes that
Ex. 6. at 2. Mr. Fowler then stated that
as long as he sold under threshold
he would stop servicing the store. Id.
A review of the compilation of
amounts he could distribute
Respondent’s sales records indicates,
pseudoephedrine without taking any
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however, that this store—the 66 Lake
Stop in Arcadia, Oklahoma—was
actually one of the smaller volume
purchasers of its pseudoephedrine
products. See Gov. Ex. 23, at 2. For
example, on May 24, 2003, the store
purchased $ 270 of products; on July 11,
2003, the store purchased $ 105: and on
August 13, 2003, the store purchased $
252. Id. The fact that this store ‘‘needed
more products that Methamphetamine
is made from,’’ begs the question of
what Mr. Fowler thought was the likely
disposition of the products he sold to
the numerous customers that were
repeatedly buying more than $ 1,000 a
month of the chemical from his firm.
Relatedly, Mr. Fowler contends that
‘‘the DEA did not warn him that he was
making suspicious sales, [or] that he
was making excessive sales’’ before
November 3, 2003. Resp. Br. at 10. See
also id. at 2 (‘‘Between September, 2001
and November 3, 2003, the DEA never
formally warned Mr. Fowler that he was
selling excessive amounts of
pseudoephedrine.’’). The suggestion that
Respondent would have stopped its
excessive sales if it had been warned is
absurd. As the Government’s
compilation of Respondent’s sales
invoices establishes, Mr. Fowler
continued to sell extraordinary
quantities of pseudoephedrine to
numerous stores for months following
the November 3, 2003 warning. Indeed,
it appears that the only reason that the
sales eventually stopped was because
Respondent’s customers ceased
purchasing the products in anticipation
of the effective date of the new
Oklahoma law which restricted the sale
of tablet-form pseudoephedrine. See
generally Gov. Ex. 23. In short, it is clear
that DEA’s warning did not register with
Mr. Fowler. I thus conclude that
Respondent lacks effective controls
against diversion and that this factor is,
by itself, sufficient to conclude that
Respondent’s continued registration
would be inconsistent with the public
interest.
Factors Two and Three—Respondent’s
Compliance With Applicable Laws and
Record of Criminal Convictions
As noted by the ALJ, Respondent has
previously been admonished for several
violations of DEA regulations pertaining
to security and recordkeeping
requirements. Moreover, while Mr.
Fowler has not been formally convicted
of a crime (because a final judgment has
yet to be entered in the state criminal
case), a jury recently found him guilty
of the state law offense of distributing
pseudoephedrine ‘‘with reckless
disregard as to how the product will be
used.’’ 63 Okl. St. Ann. section 2–
VerDate Aug<31>2005
15:09 Apr 10, 2007
Jkt 211001
333(A). I also hold that Respondent’s
distributions of pseudoephedrine
violated 21 U.S.C. 841(c)(2) (prohibiting
the possession or distribution of ‘‘a
listed chemical knowing, or having
reasonable cause to believe, that the
listed chemical will be used to
manufacture a controlled substance’’).
Accordingly, while Mr. Fowler has not
been formally convicted of a crime, I
conclude that Respondent’s record of
compliance with applicable federal and
state laws further demonstrates that
Respondent’s continued registration
would be inconsistent with the public
interest.
Factors Four and Five—Respondent’s
Experience in the Distribution of
Chemicals and Other Factors Relevant
to and Consistent With Public Health
and Safety
As explained above, Respondent’s
experience in the distribution of listed
chemicals is characterized by the
egregious and criminal misconduct of
its owner, Mr. Fowler. But even if there
was no such evidence, I would still
conclude—consistent with DEA
precedent—that Respondent’s excessive
sales to non-traditional retailers would
support a finding under factor five that
its continued registration would be
inconsistent with the public interest.
While pseudoephedrine has a
legitimate medical use as a
decongestant, its diversion into the
illicit manufacture of methamphetamine
has had pernicious effects on families
and communities throughout the nation.
Cutting off the supply source of
methamphetamine traffickers is thus of
critical importance in protecting the
public from the devastation wreaked by
this drug.
DEA orders have established that
convenience stores and gas-stations
constitute the non-traditional retail
market for legitimate consumers of
products containing this chemical. See,
e.g., Tri-County Bait Distributors, 71 FR
52160, 52161–62; D & S Sales, 71 FR at
37609; Branex, Inc., 69 FR 8682, 8690–
92 (2004). DEA has further found that
there is a substantial risk of diversion of
pseudoephedrine into the illicit
manufacture of methamphetamine when
these products are sold by nontraditional retailers. See, e.g., Joy’s
Ideas, 70 FR at 33199 (finding that the
risk of diversion was ‘‘real’’ and
‘‘substantial’’); Jay Enterprises, 70 FR
24620, 24621 (2005) (noting
‘‘heightened risk of diversion’’ should
application be granted). See also TNT
Distributors, 70 FR 12729, 12730 (2005)
(establishing that ‘‘80 to 90 percent of
ephedrine and pseudoephedrine being
used [in Tennessee] to manufacture
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18279
methamphetamine was being obtained
from convenience stores’’); Joey
Enterprises, 70 FR 76866, 76867 (2005)
(‘‘[w]hile there are no specific
prohibitions under the Controlled
Substances Act regarding the sale of
listed chemical products to [gas stations
and convenience stores], DEA has
nevertheless found that [these entities]
constitute sources for the diversion of
listed chemical products’’).
The record here likewise establishes
that there is a substantial nexus between
the sale of non-traditional list I chemical
products by non-traditional retailers and
the diversion of these products into the
illicit manufacture of
methamphetamine. Here, testimony
establishes that Max Brand
pseudoephedrine was the preferred
product of Oklahoma meth. cooks and
that this product was found in about
eighty percent of the illicit laboratories
seized by law enforcement authorities.
Tr. 180–82. The Government also
established that Max Brand pseudo was
not found in traditional retailers and
that it was distributed to non-traditional
retailers such as convenience stores and
gas stations from which meth cooks
obtained the product. See id.
Furthermore, the Government also
showed that ‘‘the vast majority of
pseudoephedrine diversion’’ in
Oklahoma occurs in the non-traditional
retail market. Id. at 216.
To protect the public from the harms
caused by methamphetamine abuse,
DEA has repeatedly revoked the
registrations of list I chemical
distributors who supplied the nontraditional market for selling quantities
of products that clearly exceeded
legitimate demand and were likely
diverted into the illicit manufacture of
methamphetamine. See T. Young
Associates, Inc., 71 FR at 60572–73; D
& S Sales, 71 FR at 37611–12; Joy’s
Ideas, 70 FR at 33198–99; Branex, Inc.,
69 FR at 8693–96. Here, the record
clearly establishes that Respondent
distributed pseudoephedrine products
in quantities that grossly exceeded
legitimate consumer demand for these
products as a decongestant. As found
above, the only plausible explanation
for these extraordinary sales is that
Respondent’s products were being
diverted into the illicit manufacture of
methamphetamine. See T. Young, 71 FR
at 60572, D & S Sales, 71 FR at 37611
(finding diversion occurred ‘‘[g]iven the
near impossibility that * * * sales were
the result of legitimate demand’’); Joy’s
Ideas, 70 FR at 33198 (finding diversion
occurred in the absence of ‘‘a plausible
explanation in the record for this
deviation from the expected norm’’).
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Federal Register / Vol. 72, No. 69 / Wednesday, April 11, 2007 / Notices
While in this case, there is substantial
evidence that Mr. Fowler distributed
pseudoephedrine with a reckless
disregard for its eventual use, such
proof is not essential to sustain the
revocation of Respondent’s registration.
A proceeding under section 304 of the
CSA is not a criminal prosecution.
Rather, its purpose is to protect the
public interest. See Leo R. Miller, 53 FR
21931, 21932 (1988).
‘‘ ‘In determining the public interest,’
Congress granted the Attorney General
broad discretion to consider any other
factor that is ‘relevant to and consistent
with the public health and safety.’’ ’ T.
Young, 71 FR at 60572 (quoting 21
U.S.C. 823(h)(5)). The statutory text of
factor five does not require that the
Government prove that a registrant or its
key employees acted with any particular
mens rea.8 As I have previously
explained, ‘‘the diversion of list I
chemicals into the illicit manufacture of
methamphetamine poses the same
threat to public health and safety
whether a registrant sells the products
knowing they will be diverted, sells
them with a reckless disregard for the
diversion, see D & S Sales, 71 FR at
37610–12, or sells them being totally
unaware that the products were being
diverted.’’ T. Young, 71 FR at 60572
(citing Joy’s Ideas, 70 FR at 33198)
(revoking registration notwithstanding
that distributor was ‘‘an unknowing and
unintentional contributor to [the]
methamphetamine problem’’).
Accordingly, Respondent’s excessive
sales of pseudoephedrine also provide
reason alone to conclude that its
continued registration would be
inconsistent with the public interest.
In sum, four of the five factors
conclusively demonstrate that
Respondent’s continued registration is
inconsistent with the public interest.
Furthermore, in accordance with 21
CFR 1316.67, I find that Respondent’s
owner engaged in egregious misconduct
and is responsible for the diversion of
massive amounts of pseudoephedrine
into the illicit manufacture of
methamphetamine. There, I conclude
that the public interest requires that
Respondent’s registration be revoked
effective immediately.
cprice-sewell on PRODPC61 with NOTICES
Order
Accordingly, pursuant to the
authority vested in me by 21 U.S.C.
823(h) & 824(a), as well as 28 CFR
0.100(b) & 0.104, I order that DEA
Certificate of Registration, 003949RPY,
8 To the extent mens rea is relevant, it is
accounted for in factor three, which directs the
consideration of a registrant’s prior conviction
record. See 21 U.S.C. 823(h)(3).
VerDate Aug<31>2005
15:09 Apr 10, 2007
Jkt 211001
issued to Rick’s Picks, L.L.C., be, and it
hereby is, revoked. I further order that
the pending application of Rick’s Picks,
L.L.C., for renewal of its registration be,
and it hereby is, denied. This order is
effective immediately.
Dated: March 30, 2007.
Michele M. Leonhart,
Deputy Administrator.
[FR Doc. E7–6759 Filed 4–10–07; 8:45 am]
BILLING CODE 4410–09–P
NATIONAL AERONAUTICS AND
SPACE ADMINISTRATION
[Notice: 07–030]
Notice of Information Collection
National Aeronautics and
Space Administration (NASA).
ACTION: Notice of information collection.
AGENCY:
SUMMARY: The National Aeronautics and
Space Administration, as part of its
continuing effort to reduce paperwork
and respondent burden, invites the
general public and other Federal
agencies to take this opportunity to
comment on proposed and/or
continuing information collections, as
required by the Paperwork Reduction
Act of 1995 (Pub. L. 104–13, 44 U.S.C.
3506(c)(2)(A)).
DATES: All comments should be
submitted within 60 calendar days from
the date of this publication.
ADDRESSES: All comments should be
addressed to Mr. Walter Kit, National
Aeronautics and Space Administration,
Washington, DC 20546–0001.
FOR FURTHER INFORMATION CONTACT:
Requests for additional information or
copies of the information collection
instrument(s) and instructions should
be directed to Mr. Walter Kit, NASA
PRA Officer, NASA Headquarters, 300 E
Street SW., JE000, Washington, DC
20546, (202) 358–1350, Walter.Kit1@nasa.gov.
SUPPLEMENTARY INFORMATION:
I. Abstract
This is an online application form for
the Exploration Systems Mission
Directorate—Space Grant Consortia
Faculty Project. NASA must select
candidates via a competitive process,
and in order to do so must collect
personal information in an application.
The voluntary respondents will be fulltime professors that are employed at a
university in the United States or Puerto
Rico.
II. Method of Collection
This information collected on the
application is needed to competitively
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select faculty to participate in the 10
week Fellowship.
III. Data
Title: Exploration Systems Mission
Directorate—Space Grant Consortia
Faculty Project.
OMB Number: 2700–XXXX.
Type of review: New Collection.
Affected Public: Individuals or
households.
Number of Respondents: 156.
Responses Per Respondent: 0.5 hour.
Annual Responses: 156.
Annual Burden Hours: 80.
IV. Request for Comments
Comments are invited on: (1) Whether
the proposed collection of information
is necessary for the proper performance
of the functions of NASA, including
whether the information collected has
practical utility; (2) the accuracy of
NASA’s estimate of the burden
(including hours and cost) of the
proposed collection of information; (3)
ways to enhance the quality, utility, and
clarity of the information to be
collected; and (4) ways to minimize the
burden of the collection of information
on respondents, including automated
collection techniques or the use of other
forms of information technology.
Comments submitted in response to
this notice will be summarized and
included in the request for OMB
approval of this information collection.
They will also become a matter of
public record.
Gary Cox,
Deputy Chief Information Officer (Acting).
[FR Doc. E7–6772 Filed 4–10–07; 8:45 am]
BILLING CODE 7510–13–P
NUCLEAR REGULATORY
COMMISSION
[Docket Nos. 050–00315, 050–00316;
License Nos. DPR–58 & DPR–74 EA–06–
295]
In the Matter of Indiana Michigan
Power Company D.C. Cook Nuclear
Power Plant; Confirmatory Order
Modifying License (Effective
Immediately)
I
Indiana Michigan Power Company
(I&M or Licensee) is the holder of
Facility Operating License Nos. DPR–58
and DPR–74 issued by the U.S. Nuclear
Regulatory Commission (NRC or
Commission) pursuant to 10 CFR Part
50 on October 25, 1974 and December
23, 1977, respectively. The licenses
authorize the operation of the D.C. Cook
nuclear power plant units 1 & 2 in
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11APN1
Agencies
[Federal Register Volume 72, Number 69 (Wednesday, April 11, 2007)]
[Notices]
[Pages 18275-18280]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E7-6759]
-----------------------------------------------------------------------
DEPARTMENT OF JUSTICE
Drug Enforcement Administration
[Docket No. 05-8]
Rick's Picks, L.L.C.; Revocation of Registration
On October 7, 2004, the Deputy Assistant Administrator, Office of
Diversion Control, Drug Enforcement Administration, issued an Order to
Show Cause to Rick's Picks, L.L.C. (Respondent), of Moore, Oklahoma.
The Show Cause Order proposed the revocation of Respondent's DEA
Certificate of Registration, 003949RPY, as a distributor of list I
chemicals, on the ground that its continued registration was
inconsistent with the public interest. Show Cause Order at 1 (citing 21
U.S.C. 823(h)).
The Show Cause Order incorporated the allegations of a show cause
order which was initiated by the Oklahoma State Bureau of Narcotics and
Dangerous Drugs Control; the latter order proposed the denial of
Respondent's application for a state registration to distribute
pseudoephedrine products that are Schedule V drugs under State law, as
well as the revocation of Respondent's state registration to distribute
pseudoephedrine products which are not scheduled under state law. Id.
at 2. Specifically, the state show cause order alleged that Respondent
and its owner, Rick D. Fowler, ``have a history of selling very large
amounts of pseudoephedrine under suspicious and questionable
circumstances, and with great negligence and reckless disregard for
whether this product would be used in the clandestine manufacture of
methamphetamine,'' and that Respondent, and its owner, had engaged in
this activity notwithstanding ``numerous warnings from . . . DEA
officials that Respondent's sales were fueling illicit methamphetamine
laboratories.'' Id.
Relatedly, the State show cause order alleged that from January
2002 through April 2004, Respondent sold more than $ 2.2 million of Max
Brand (for a total of nearly 10.5 million tablets), a product in which
pseudoephedrine is the single active ingredient and which is the
``preferred choice [of] methamphetamine cooks.'' Id. at 4-5. The state
show cause order also alleged that Respondent had brokered the sale of
approximately 400,000 pseudoephedrine tablets for D & E Pharmaceutical.
Id. at 5. The DEA Show Cause Order then repeated ten different
allegations made in the state show cause order which asserted specific
instances in which Respondent had sold extraordinary quantities of
pseudoephedrine to convenience stores, gas stations and other non-
traditional retailers of this product, and that Respondent had failed
to report any of these transactions to DEA. Id. at 6-8.
The State show cause order further alleged that pseudoephedrine
distributed by Respondent had been found at twenty-two methamphetamine
dumpsites. Id. at 8. Finally, the DEA Show Cause Order alleged that in
November 2003, DEA had conducted an inspection of Respondent during
which numerous recordkeeping violations were observed. Id. at 9.
Respondent requested a hearing on the allegations. The matter was
assigned
[[Page 18276]]
to Administrative Law Judge (ALJ) Mary Ellen Bittner, who conducted a
hearing in Oklahoma City, Oklahoma, on January 10 and 11, 2006. At the
hearing, the Government introduced both testimonial and documentary
evidence; Respondent introduced only documentary evidence. Both parties
submitted post-hearing briefs.
On August 9, 2006, the ALJ issued her decision. In that decision,
the ALJ concluded that Respondent's continued registration would be
inconsistent with the public interest and recommended that its
registration be revoked. Neither party filed exceptions.
Having considered the record as a whole, I hereby issue this
decision and final order. I adopt the ALJ's findings of fact and
conclusions of law in their entirety. For the reasons set forth below,
I hold that Respondent's continued registration would be inconsistent
with the public interest and therefore revoke its registration and deny
its pending application for renewal.
Findings
Respondent, an Oklahoma corporation, is a distributor of assorted
merchandise to convenience stores, gas stations, and other small
retailers in that State. Respondent's sole owner is Mr. Rickey Fowler.
ALJ Dec. at 15.
Respondent currently holds DEA Certificate of Registration,
003949RPY, which authorizes it to distribute list I chemicals. Gov. Ex.
1. While Respondent's registration certificate states that its
registration expired on April 30, 2005, the record indicates that
Respondent filed a timely renewal application. Tr. 24. Therefore,
Respondent's registration remains in effect until the conclusion of
this proceeding. See 5 U.S.C. 558(c).
Methamphetamine and the Market for List I Chemicals
Pseudoephedrine is lawfully marketed under the federal Food, Drug
and Cosmetic Act for over-the-counter use as a decongestant.
Pseudoephedrine is, however, also regulated as a list I chemical under
the Controlled Substances Act because it is easily extracted from non-
prescription products and used in the illicit manufacture of
methamphetamine, a Schedule II controlled substance. See 21 U.S.C.
802(34); 21 CFR 1308.12(d).
Methamphetamine ``is a powerful and addictive central nervous
system stimulant.'' T. Young Associates, Inc., 71 FR 60567 (2006). The
illegal manufacture and abuse of methamphetamine pose a grave threat to
this country. Methamphetamine abuse has destroyed numerous lives and
families and ravaged communities. Moreover, because of the toxicity of
the chemicals used in producing the drug, its illicit manufacture
causes serious environmental harms. Id.
Methamphetamine abuse has been an especially serious problem in the
State of Oklahoma. In 1999, law enforcement authorities seized 391
illicit laboratories/dumpsites in the State; in 2003 (the last full
year before the State enacted laws restricting the distribution of
pseudoephedrine), authorities seized 1091 illicit laboratories/
dumpsites. See Gov. Exs. 7 & 11. Moreover, in 2004, there were still
659 seizures. See Gov. Ex. 12. According to a senior agent for the
Oklahoma Bureau of Narcotics, Max Brand in tablet form, a product in
which pseudoephedrine (60 mg.) is the single active ingredient, is the
preferred product of the State's illicit methamphetamine cooks.\1\ See
also Tr. 46 & 180.
---------------------------------------------------------------------------
\1\ In response to the methamphetamine problem, effective April
6, 2004, Oklahoma made pseudoephedrine in tablet form a Schedule V
controlled substance. Pseudoephedrine in liquid, liquid-filled
capsules, and gel caps is, however, exempt from the requirement
provided it is not the only active ingredient in the product. See 63
Okl. St. Ann. section 2-212.
---------------------------------------------------------------------------
In the course of adjudicating numerous cases, DEA has acquired
substantial expertise pertaining to the market for list I chemical
products containing pseudoephedrine. Accordingly, pursuant to 5 U.S.C.
556(e), I take official notice of the following facts related to the
market for pseudoephedrine.\2\
---------------------------------------------------------------------------
\2\ Under the Administrative Procedure Act, ``[a]gencies may
take official notice of facts at any stage in a proceeding-even in
the final decision.'' Attorney General's Manual on the
Administrative Procedure Act 80 (1946) ( Wm. W. Gaunt & Sons, Inc.,
reprint 1979). In accordance with the Act, Respondent may request a
reopening of the proceeding to contest the facts of which I am
taking official notice by filing a request with supporting
affidavits no later than fifteen days after service of this order.
---------------------------------------------------------------------------
According to Jonathan Robbin, an expert in statistical analysis of
demographic, economic, geographic and survey data, ``over 97% of all
sales of non-prescription drug products occur in drug stores and
pharmacies, supermarkets, large discount merchandisers and electronic
shopping and mail order houses.'' T. Young, 71 FR at 60568. Moreover,
``sales of non-prescription drugs by convenience stores (including both
those that sell and do not sell gasoline), account for only 2.2% of the
overall sales of all convenience stores that handle the line and only
0.7% of the total sales of all convenience stores.'' Id.
Based on his study of U.S. Government Economic Census Data,
information obtained from the National Association of Convenience
Stores, and commercially available point of sale transaction data, Mr.
Robbin has constructed a model of the traditional market for retail
sales of pseudoephedrine. See id. According to Mr. Robbin, ``sales of
pseudoephedrine account for only about 2.6% of the sales of health and
beauty care products in convenience stores and only 0.05% of total in-
store (non-gasoline) sales.'' Id.
Moreover, ``the normal expected retail sale of pseudoephedrine
(Hcl) tablets in a convenience store may range between $ 0 and $ 40 per
month, with an average of $ 20.60 per month.'' Id. According to Mr.
Robbin, a monthly retail sale at a non-traditional retailer of ``$ 60
of pseudoephedrine would occur less than one in 1,000 times in random
sampling.'' Id. Moreover, a monthly retail sale of ``$ 100 in
pseudoephedrine would occur about once in a million times in random
sampling.'' Id.
Findings Pertaining To Respondent
Respondent first became registered to distribute list I chemicals
in January 1999. Prior to becoming registered, DEA Diversion
Investigators (DIs) conducted a pre-registration investigation. During
this visit, the DIs discussed with Mr. Fowler the recordkeeping
requirements imposed by federal law and regulations. Tr. 32-33. The DIs
also provided Mr. Fowler with DEA notices that discussed suspicious
transactions and advised that certain list I chemical products
including pseudoephedrine were being diverted into the illicit
manufacture of methamphetamine. Id. at 34. One of the notices
specifically stated that ``[t]he exemption from certain recordkeeping
and reporting requirements for below threshold transactions . . . does
not reduce the risk of criminal liability.'' Gov. Ex. 3. This notice
also advised Mr. Fowler to ``[r]eport all suspicious orders to your
nearest DEA office immediately.'' Id.
The DIs, however, also gave Mr. Fowler a handout listing required
reports. See Resp. Ex. 18, Tr. 64. More specifically, this document
stated that reports were required for ``[a]ny regulated transaction
involving an extraordinary quantity of a Listed Chemical,'' ``[a]ny
regulated transaction involving an uncommon method of payment or
delivery,'' and ``[a]ny regulated transaction involving any other
circumstances that the regulated person (supplier) believes may
indicate that the List (sic) Chemical will be used in the illicit
production of controlled substances.'' Resp. Ex. 18.
In September 2001, DEA DIs returned to Respondent for a scheduled
[[Page 18277]]
inspection. Among other things, the DIs determined that Respondent was
storing list I chemicals in a trailer at a boat storage and not at its
registered location. Id. at 37. The DIs also found that Respondent was
in violation of recordkeeping requirements because its receiving
invoices did not include the date that products were received and its
sales invoices did not indicate package size. Id. at 38. Respondent's
owner was issued a letter admonishing him for the violations. Resp. Ex.
2. Subsequently, Mr. Fowler wrote to one of the DIs advising of changes
Respondent would make in its recordkeeping; at that time, DEA took no
further action. ALJ Dec. at 16.
On November 3, 2003, DEA DIs conducted another inspection of
Respondent. The DIs determined that while Respondent was now properly
storing its list I chemical products, it was still violating the
recordkeeping requirements. See id. at 16-17. DEA issued Respondent an
additional letter of admonition. Tr. 41. During this visit, DEA also
obtained Respondent's receiving and sales invoices for the period from
January 1, 2002, through November 1, 2003. Id. at 261; Resp. Ex. 25.\3\
---------------------------------------------------------------------------
\3\ On April 7, 2004, a DEA DI again returned to Respondent to
discuss the then-recently enacted state legislation which scheduled
pseudoephedrine in tablet form. During this visit, the DI conducted
a closing inventory. ALJ Dec. at 17.
---------------------------------------------------------------------------
In May 2004, law enforcement authorities obtained a warrant and
executed a search of Respondent. Based on records obtained during the
search, as well as the records obtained during the November 2003
inspection, DEA investigators compiled a spreadsheet of Respondent's
purchases of pseudoephedrine. Gov. Ex. 21; Tr. 187. According to this
document, between January 28, 2002, and March 6, 2004, Respondent had
purchased 10,062,144 tablets of Max Brand pseudoephedrine at a
wholesale price of $ 941,072.20. Id. Moreover, during the 2003 calendar
year, Respondent purchased nearly six million tablets at a wholesale
price of $ 564,884.20. Id. Furthermore, between January 5, 2004, and
March 6, 2004 (shortly before the Oklahoma statute scheduling tablet-
form pseudoephedrine became effective), Respondent purchased
approximately 1.8 million tablets at a wholesale price of $ 173,004.
Id.
DEA investigators also compiled a spreadsheet of Respondent's
pseudoephedrine sales. See Gov. Ex. 23. This 102 page document lists
Respondent's sales to each store by product size and date. The document
shows that Respondent repeatedly made monthly sales of a $ 1,000 or
more of pseudoephedrine products to the great majority of the
stores.\4\ See generally id.
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\4\ One of the DIs testified that her review of Respondent's
records showed that its sales of pseudoephedrine constituted eighty-
five percent of its business. ALJ Dec. at 17. The Government also
introduced evidence that Respondent brokered the sale of substantial
amounts of ``Bolt'' brand pseudoephedrine directly from its
manufacturer to various stores. Tr. 273-276; Gov. Ex. 24, at 5-8.
---------------------------------------------------------------------------
For example, from January 2002 through April 6, 2004, Respondent
sold $ 62,658.00 (and brokered the sale of $ 7,013) of pseudoephedrine
to Bernhardt's, a convenience store in Pharoah, Oklahoma. Gov. Ex. 24,
at 5. During the same period, Respondent sold $ 50,256 (and brokered
the sale of $ 7,015) of pseudoephedrine to Dock's General Store in
Council Hill, Oklahoma, and sold $ 44,640 (and brokered the sale of $
7,015) of the chemical to Dock's General Store in Leonard, Oklahoma.
Id. at 6-7. Both of these establishments were bait and tackle shops.
Tr. 269-71. Respondent also sold $ 37,116 (and brokered the sale of $
4,676) of the chemical to Kern's Korner Grocery in Henryetta, Oklahoma.
Gov. Ex. 24, at 8. Furthermore, from January 2002 through December
2002, Respondent sold $ 11,880 of pseudoephedrine to the Funky Munky, a
head shop located in McAlester, Oklahoma. Id. at 9; see also Tr. 273.
The record also establishes that between February 2002 and March
2004, Respondent sold $ 97,026 (and 468,144 tablets) of pseudoephedrine
to five stores in Poteau, a small city in eastern Oklahoma. Of
significance among these customers, Respondent sold $ 30,672 to Babe's
Place and $ 37,590 to the Tote-A-Poke 1. Gov. Ex. 24, at 3.
It also sold $14,040 to Burkes Friendly Store; all of the sales to
Burkes occurred between February 2002 and March 2003. Gov. Ex. 23, at
15-16.
The above per-store figures are based on Respondent's wholesale
prices. Several of Respondent's exhibits indicate that the suggested
retail price was typically twice the wholesale price. See Resp. Exh.
20, at 19; Resp. Ex. 19. Ultimately, even if Respondent's customers
sold the products at far less than the suggested retail prices, their
sales of these products so greatly exceeded the monthly expected sales
range of $ 0 to $ 40, with an average of $ 20.60, that the probability
that the products were being purchased to meet legitimate consumer
demand for use as a decongestant is infinitesimal. Indeed, as DEA's
expert has testified, a monthly retail sale of $ 100 in pseudoephedrine
to meet legitimate demand would occur about once in a million times in
random sampling. Here, where there are numerous stores to which
Respondent sold repeatedly $ 1,000 or more per month at wholesale
prices, the only plausible explanation is that the products were being
diverted into the illicit manufacture of methamphetamine.\5\ I thus
find that substantially all of Respondent's products were being
diverted.
---------------------------------------------------------------------------
\5\ During cross-examination, Respondent's counsel elicited
testimony from a Government witness that a few of the stores it sold
to were located on highways--thus suggesting that the sales at these
stores were to meet legitimate consumer demand. Tr. 201-02. This
testimony does not persuade me that Respondent's products were being
sold to meet legitimate demand. The ALJ found that Respondent had
more than 200 customers, see ALJ Dec. at 18; Respondent's line of
cross-examination begs the question: What about the other 200 plus
stores? Indeed, the ALJ found that ``some of Respondent's customers
were convicted of criminal charges involving the diversion of
pseudoephedrine.'' Id.
---------------------------------------------------------------------------
The ALJ further credited the testimony of a DEA investigator that
``some of Respondent's customers engaged in practices that the DEA
considers suspicious.'' ALJ at 18. More specifically, these practices
included: (1) Ordering only single-entity pseudoephedrine rather than a
variety of pseudoephedrine and other over-the-counter drug products,
(2) selling single-entity products that are marketed in large
quantities and not in blister packs, (3) selling products that have
only been on the market for a few years and which receive little
advertising, and (4) purchasing large quantities of pseudoephedrine
throughout the year by establishments that traditionally do not sell
large quantities of these products and do little or no marketing of
them.\6\ ALJ at 18, Tr. 349-51.
---------------------------------------------------------------------------
\6\ Most of these indicia were published by DEA in February
1999. See Suspicious Orders Task Force, Report to the U.S. Attorney
General Appendix A (1999). The indicia were re-published in the June
2002 Chemical Handler's Manual. See DEA, Chemical Handler's Manual--
A Guide to Chemical Control Regulations 40-43 (June 2002).
---------------------------------------------------------------------------
The ALJ further found that ``Respondent never sold more than the
[1000 grams] threshold amount to any one customer in a calendar
month.'' ALJ at 20. The ALJ also found that Respondent's owner twice
``reported a suspicious sale to'' DEA. Id. According to the record, on
October 8, 2003, Mr. Fowler reported that while servicing a store the
previous day, ``the store clerk made a comment that she needed products
that Methamphetamine is made from.'' Resp. Ex. 6, at p. 2. Mr. Fowler
further wrote that he had ``suspended sales of all pseudo ephedrine
products to this store due to this comment,'' and that he would ``not
service this store in the future with any cold medications containing
pseudo ephedrine.'' Id. Approximately, a month
[[Page 18278]]
later Mr. Fowler also reported that he had been contacted by a person
who wanted to come to his premises to purchase products but Mr. Fowler
advised him that his firm ``did not do business this way.'' Id. at 3.
Mr. Fowler further stated that the address given by this person was
non-existent and that he had determined that the business was not
legitimate.\7\ Id.
---------------------------------------------------------------------------
\7\ While Respondent introduced several form letters to
customers purporting to impose requirements for the sale of
pseudoephedrine, Resp. Exs. 11-13, as the ALJ noted, ``Respondent
did not call any witnesses at the hearing, and there is no evidence
as to whether such letters were mailed to Respondent's customers.''
ALJ Dec. at 19.
---------------------------------------------------------------------------
On November 14, 2005, the Cleveland County, Oklahoma, District
Attorney filed a felony information charging Mr. Fowler with criminal
racketeering under Oklahoma law. Gov. Ex. 42. More specifically, the
information alleged that ``between January 2002 and April 2004,''
Fowler ``was willfully, knowingly and criminally associated with an
enterprise,'' which consisted of himself, ``individually, and as the
owner of Rick Picks,'' the affairs of which ``were to distribute
pseudoephedrine, a precursor in the manufacturing of methamphetamine,
with reckless disregard for how the product was going to be used in
violation of 63 O.S. 2-333(A).'' Id. I further take official notice of
the fact that on October 16, 2006, the State filed a second amended
felony information charging Respondent with the ``unlawful distribution
of pseudoephedrine with reckless disregard for how it was going to be
used.'' Finally, I take official notice of the fact that on February 9,
2007, a jury found Mr. Fowler guilty of the crime charged in the second
amended information. See Docket Sheet, State v. Fowler, No. CF-2005-
1651, Cleveland County, Oklahoma, District Court.
Discussion
Section 304(a) of the Controlled Substances Act provides that a
registration to distribute a list I chemical ``may be suspended or
revoked * * * upon a finding that the registrant * * * has committed
such acts as would render his registration under section 823 of this
title inconsistent with the public interest as determined under such
section.'' 21 U.S.C. 824(a)(4). In making this determination, Congress
directed that I consider the following factors:
(1) Maintenance by the [registrant] of effective controls
against diversion of listed chemicals into other than legitimate
channels;
(2) compliance by the applicant with applicable Federal, State,
and local law;
(3) any prior conviction record of the applicant under Federal
or State laws relating to controlled substances or to chemicals
controlled under Federal or State law;
(4) any past experience of the applicant in the manufacture and
distribution of chemicals; and
(5) such other factors as are relevant to and consistent with
the public health and safety.
Id. section 823(h).
``These factors are considered in the disjunctive.'' Joy's Ideas,
70 FR 33195, 33197 (2005). I may rely on any one or a combination of
factors, and may give each factor the weight I deem appropriate in
determining whether a registration should be revoked or an application
for renewal of a registration should be denied. See, e.g., David M.
Starr, 71 FR 39367, 39368 (2006); Energy Outlet, 64 FR 14269 (1999).
Moreover, I am ``not required to make findings as to all of the
factors.'' Hoxie v. DEA, 419 F.3d 477, 482 (6th Cir. 2005); Morall v.
DEA, 412 F.3d 165, 173-74 (D.C. Cir. 2005). In this case, I hold that
factors one, two, four, and five overwhelmingly establish that
Respondent's continued registration would be ``inconsistent with the
public interest.'' 21 U.S.C. 823(h). Accordingly, I further hold that
Respondent's registration should be revoked and its pending application
for renewal should be denied.
Factor One--Maintenance of Effective Controls Against Diversion
I concur with the ALJ's conclusion that the record does not
establish that Respondent fails to provide adequate physical security
for list I chemicals. However, ``'[p]rior agency rulings have applied a
more expansive view of factor one than mere physical security.'' ' D &
S Sales, 71 FR 37607, 37610 (2006) (quoting OTC Distribution Co., 68 FR
70538, 70542 (2003)). Relatedly, I have previously held that a
registrant is ``required to exercise a high degree of care in
monitoring its customers' purchases.'' D & S Sales, 71 FR at 37610.
Respondent argues that he maintains effective controls against
diversion because he obtained proof of identity from his customers and
only distributed to ``legitimate store[s],'' Resp. Statement of
Supporting Reasons 9 [hereinafter Resp. Br.], he maintained adequate
and retrievable records, id., and he ``did not fail to report
suspicious sales because he was only required to report suspicious
regulated transactions,'' i.e., transactions that exceeded the 1,000
grams threshold. Id. at 11 (citing 21 U.S.C. 830(b)(1) and 21 CFR
1310.05(a)(1)).
Respondent apparently believes that as long as he sold under
threshold amounts he could distribute pseudoephedrine without taking
any further steps to determine the ultimate disposition of his
products. Respondent's understanding is mistaken. Congress's imposition
of recordkeeping and reporting requirements for regulated transactions
does not mean that one can engage in below-threshold transactions
without any further obligation to determine whether the products are
likely to be diverted. Indeed, DEA has found that products which have
been distributed to non-traditional retailers in sub-threshold
transactions are routinely diverted. Contrary to Respondent's view, the
threshold provisions pertaining to regulated transactions do not create
a safe harbor which allows a registrant to sell list I chemicals
without any further duty to investigate how the products are being
used.
Respondent further contends that ``[t]here was no evidence
presented that [it] had actual knowledge [that] any customer was
diverting pseudoephedrine for the manufacture of methamphetamine.'' Id.
at 10. In short, Respondent raises the ostrich defense.
Congress, however, has rejected the ostrich defense in creating
criminal liability under 21 U.S.C. 841(c)(2), and I have previously
rejected this defense as incompatible with the purpose of proceedings
under 21 U.S.C. 823 and 824, which are brought to protect the public
interest. See D & S Sales, 71 FR at 37612; T. Young Associates, 71 FR
at 60572. As D & S Sales explained: ``Burying one's head in the sand
while his firm's products are being diverted may allow one to maximize
profits. But it is manifestly inconsistent with public health and
safety.'' 71 FR at 37612. More recently, I revoked a registration
holding--albeit in the context of analyzing factors four and five--that
a registrant's lack of ``any intent to divert or to sell to customers
who were diverting to the illicit manufacture of methamphetamine is
irrelevant.'' T. Young, 71 FR at 60572. See also Joy's Ideas, 70 FR at
33198 (revoking registration notwithstanding that distributor was ``an
unknowing and unintentional contributor to [the] methamphetamine
problem.'').
Respondent's owner also contends that he maintained adequate
controls because he ``reported suspicious activities to the DEA in the
past.'' Resp. Br. at 9. According to the record, Mr. Fowler reported an
encounter he had during which a store clerk informed him ``that she
needed products that Methamphetamine is made from.'' Resp. Ex. 6. at 2.
Mr. Fowler then stated that he would stop servicing the store. Id.
A review of the compilation of Respondent's sales records
indicates,
[[Page 18279]]
however, that this store--the 66 Lake Stop in Arcadia, Oklahoma--was
actually one of the smaller volume purchasers of its pseudoephedrine
products. See Gov. Ex. 23, at 2. For example, on May 24, 2003, the
store purchased $ 270 of products; on July 11, 2003, the store
purchased $ 105: and on August 13, 2003, the store purchased $ 252. Id.
The fact that this store ``needed more products that Methamphetamine is
made from,'' begs the question of what Mr. Fowler thought was the
likely disposition of the products he sold to the numerous customers
that were repeatedly buying more than $ 1,000 a month of the chemical
from his firm.
Relatedly, Mr. Fowler contends that ``the DEA did not warn him that
he was making suspicious sales, [or] that he was making excessive
sales'' before November 3, 2003. Resp. Br. at 10. See also id. at 2
(``Between September, 2001 and November 3, 2003, the DEA never formally
warned Mr. Fowler that he was selling excessive amounts of
pseudoephedrine.''). The suggestion that Respondent would have stopped
its excessive sales if it had been warned is absurd. As the
Government's compilation of Respondent's sales invoices establishes,
Mr. Fowler continued to sell extraordinary quantities of
pseudoephedrine to numerous stores for months following the November 3,
2003 warning. Indeed, it appears that the only reason that the sales
eventually stopped was because Respondent's customers ceased purchasing
the products in anticipation of the effective date of the new Oklahoma
law which restricted the sale of tablet-form pseudoephedrine. See
generally Gov. Ex. 23. In short, it is clear that DEA's warning did not
register with Mr. Fowler. I thus conclude that Respondent lacks
effective controls against diversion and that this factor is, by
itself, sufficient to conclude that Respondent's continued registration
would be inconsistent with the public interest.
Factors Two and Three--Respondent's Compliance With Applicable Laws and
Record of Criminal Convictions
As noted by the ALJ, Respondent has previously been admonished for
several violations of DEA regulations pertaining to security and
recordkeeping requirements. Moreover, while Mr. Fowler has not been
formally convicted of a crime (because a final judgment has yet to be
entered in the state criminal case), a jury recently found him guilty
of the state law offense of distributing pseudoephedrine ``with
reckless disregard as to how the product will be used.'' 63 Okl. St.
Ann. section 2-333(A). I also hold that Respondent's distributions of
pseudoephedrine violated 21 U.S.C. 841(c)(2) (prohibiting the
possession or distribution of ``a listed chemical knowing, or having
reasonable cause to believe, that the listed chemical will be used to
manufacture a controlled substance''). Accordingly, while Mr. Fowler
has not been formally convicted of a crime, I conclude that
Respondent's record of compliance with applicable federal and state
laws further demonstrates that Respondent's continued registration
would be inconsistent with the public interest.
Factors Four and Five--Respondent's Experience in the Distribution of
Chemicals and Other Factors Relevant to and Consistent With Public
Health and Safety
As explained above, Respondent's experience in the distribution of
listed chemicals is characterized by the egregious and criminal
misconduct of its owner, Mr. Fowler. But even if there was no such
evidence, I would still conclude--consistent with DEA precedent--that
Respondent's excessive sales to non-traditional retailers would support
a finding under factor five that its continued registration would be
inconsistent with the public interest.
While pseudoephedrine has a legitimate medical use as a
decongestant, its diversion into the illicit manufacture of
methamphetamine has had pernicious effects on families and communities
throughout the nation. Cutting off the supply source of methamphetamine
traffickers is thus of critical importance in protecting the public
from the devastation wreaked by this drug.
DEA orders have established that convenience stores and gas-
stations constitute the non-traditional retail market for legitimate
consumers of products containing this chemical. See, e.g., Tri-County
Bait Distributors, 71 FR 52160, 52161-62; D & S Sales, 71 FR at 37609;
Branex, Inc., 69 FR 8682, 8690-92 (2004). DEA has further found that
there is a substantial risk of diversion of pseudoephedrine into the
illicit manufacture of methamphetamine when these products are sold by
non-traditional retailers. See, e.g., Joy's Ideas, 70 FR at 33199
(finding that the risk of diversion was ``real'' and ``substantial'');
Jay Enterprises, 70 FR 24620, 24621 (2005) (noting ``heightened risk of
diversion'' should application be granted). See also TNT Distributors,
70 FR 12729, 12730 (2005) (establishing that ``80 to 90 percent of
ephedrine and pseudoephedrine being used [in Tennessee] to manufacture
methamphetamine was being obtained from convenience stores''); Joey
Enterprises, 70 FR 76866, 76867 (2005) (``[w]hile there are no specific
prohibitions under the Controlled Substances Act regarding the sale of
listed chemical products to [gas stations and convenience stores], DEA
has nevertheless found that [these entities] constitute sources for the
diversion of listed chemical products'').
The record here likewise establishes that there is a substantial
nexus between the sale of non-traditional list I chemical products by
non-traditional retailers and the diversion of these products into the
illicit manufacture of methamphetamine. Here, testimony establishes
that Max Brand pseudoephedrine was the preferred product of Oklahoma
meth. cooks and that this product was found in about eighty percent of
the illicit laboratories seized by law enforcement authorities. Tr.
180-82. The Government also established that Max Brand pseudo was not
found in traditional retailers and that it was distributed to non-
traditional retailers such as convenience stores and gas stations from
which meth cooks obtained the product. See id. Furthermore, the
Government also showed that ``the vast majority of pseudoephedrine
diversion'' in Oklahoma occurs in the non-traditional retail market.
Id. at 216.
To protect the public from the harms caused by methamphetamine
abuse, DEA has repeatedly revoked the registrations of list I chemical
distributors who supplied the non-traditional market for selling
quantities of products that clearly exceeded legitimate demand and were
likely diverted into the illicit manufacture of methamphetamine. See T.
Young Associates, Inc., 71 FR at 60572-73; D & S Sales, 71 FR at 37611-
12; Joy's Ideas, 70 FR at 33198-99; Branex, Inc., 69 FR at 8693-96.
Here, the record clearly establishes that Respondent distributed
pseudoephedrine products in quantities that grossly exceeded legitimate
consumer demand for these products as a decongestant. As found above,
the only plausible explanation for these extraordinary sales is that
Respondent's products were being diverted into the illicit manufacture
of methamphetamine. See T. Young, 71 FR at 60572, D & S Sales, 71 FR at
37611 (finding diversion occurred ``[g]iven the near impossibility that
* * * sales were the result of legitimate demand''); Joy's Ideas, 70 FR
at 33198 (finding diversion occurred in the absence of ``a plausible
explanation in the record for this deviation from the expected norm'').
[[Page 18280]]
While in this case, there is substantial evidence that Mr. Fowler
distributed pseudoephedrine with a reckless disregard for its eventual
use, such proof is not essential to sustain the revocation of
Respondent's registration. A proceeding under section 304 of the CSA is
not a criminal prosecution. Rather, its purpose is to protect the
public interest. See Leo R. Miller, 53 FR 21931, 21932 (1988).
`` `In determining the public interest,' Congress granted the
Attorney General broad discretion to consider any other factor that is
`relevant to and consistent with the public health and safety.'' ' T.
Young, 71 FR at 60572 (quoting 21 U.S.C. 823(h)(5)). The statutory text
of factor five does not require that the Government prove that a
registrant or its key employees acted with any particular mens rea.\8\
As I have previously explained, ``the diversion of list I chemicals
into the illicit manufacture of methamphetamine poses the same threat
to public health and safety whether a registrant sells the products
knowing they will be diverted, sells them with a reckless disregard for
the diversion, see D & S Sales, 71 FR at 37610-12, or sells them being
totally unaware that the products were being diverted.'' T. Young, 71
FR at 60572 (citing Joy's Ideas, 70 FR at 33198) (revoking registration
notwithstanding that distributor was ``an unknowing and unintentional
contributor to [the] methamphetamine problem''). Accordingly,
Respondent's excessive sales of pseudoephedrine also provide reason
alone to conclude that its continued registration would be inconsistent
with the public interest.
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\8\ To the extent mens rea is relevant, it is accounted for in
factor three, which directs the consideration of a registrant's
prior conviction record. See 21 U.S.C. 823(h)(3).
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In sum, four of the five factors conclusively demonstrate that
Respondent's continued registration is inconsistent with the public
interest. Furthermore, in accordance with 21 CFR 1316.67, I find that
Respondent's owner engaged in egregious misconduct and is responsible
for the diversion of massive amounts of pseudoephedrine into the
illicit manufacture of methamphetamine. There, I conclude that the
public interest requires that Respondent's registration be revoked
effective immediately.
Order
Accordingly, pursuant to the authority vested in me by 21 U.S.C.
823(h) & 824(a), as well as 28 CFR 0.100(b) & 0.104, I order that DEA
Certificate of Registration, 003949RPY, issued to Rick's Picks, L.L.C.,
be, and it hereby is, revoked. I further order that the pending
application of Rick's Picks, L.L.C., for renewal of its registration
be, and it hereby is, denied. This order is effective immediately.
Dated: March 30, 2007.
Michele M. Leonhart,
Deputy Administrator.
[FR Doc. E7-6759 Filed 4-10-07; 8:45 am]
BILLING CODE 4410-09-P