Premier Holdings, Inc.; Denial of Application, 59834-59837 [E6-16756]
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59834
Federal Register / Vol. 71, No. 196 / Wednesday, October 11, 2006 / Notices
commercial carrier to distribute to a
non-regulated person nine grams or
more of pseudoephedrine in the course
of a calendar month engages in a
regulated transaction. See 21 U.S.C.
802(39)(A)(iv), id. section 830(b)(3); 21
CFR 1310.03(c), id. 1310.04(f). Federal
law further provides that ‘‘[i]t is the
duty of each regulated person who
engages in a regulated transaction to
identify each other party to the
transaction.’’ 21 U.S.C. 830(a)(3); see
also 21 CFR 1310.07. Under DEA’s
regulations, ‘‘[f]or sales to individuals
* * * the type of documents and other
evidence of proof must consist of at
least a signature of the purchaser, a
driver’s license and one other form of
identification.’’ 21 CFR 1310.07(d).2
It seems highly likely that
Respondent’s sales would frequently
exceed the threshold. Most significantly,
Respondent does not appear to have in
place any procedures to verify the
identity of its customers, most of which
are located outside of Tennessee and at
a great distance from Respondent’s three
salespersons. I thus find that
Respondent lacks effective controls to
prevent diversion. While this factor is
reason alone to conclude that granting
Respondent’s application would be
inconsistent with the public interest, a
discussion of factor five is also
warranted.
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Factor Five—Other Factors That Are
Relevant to and Consistent With Public
Health and Safety
The record establishes that
Respondent’s proposed customers are
not participants in the traditional retail
market for pseudoephedrine products.
See, e.g. D & S Sales, 71 FR 37607,
37608–09 (2006); Joy’s Ideas, 70 FR at
33197. Indeed, dive shops and paint ball
facilities seem to be an even less likely
source for legitimate consumer
purchases of pseudoephedrine than
convenience stores and gas stations,
establishments which DEA has
repeatedly found to be ‘‘sources for the
diversion of listed chemical products.’’
Joey Enterprises, 70 FR 76866, 76867
(2005). Moreover, Respondent’s
customer list included numerous
individuals with no listed business
affiliation. Why these individuals would
need to purchase pseudoephedrine from
a wholesaler rather than a retailer is not
clear.
2 For sales to a new customer that is ‘‘not an
individual * * *, the regulated person shall
establish the identity of the authorized purchasing
agent or agents and have on file that person’s
signature, electronic password, or other
identification.’’ 21 CFR 1310.07(e). A regulated
person must also ‘‘verify the existence and apparent
validity of a business entity.’’ Id. at 1310.07(b).
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DEA final orders have repeatedly
recognized that ‘‘there is a substantial
risk of diversion of List I chemicals into
the illicit manufacture of
methamphetamine when these products
are sold by non-traditional retailers.’’
Tri-County Bait Distributors, 71 FR
52160, 52164 (2006). See also Joy’s
Ideas, 70 FR at 33199 (finding that the
risk of diversion was ‘‘real, substantial
and compelling’’); Jay Enterprises, 70 FR
at 24621 (noting ‘‘heightened risk of
diversion’’ should application be
granted). Under DEA precedents, an
applicant’s proposal to sell into the nontraditional market weighs heavily
against the granting of a registration
under factor five. So too here.
I acknowledge that Respondent
proposed to sell only name brand
pseudoephedrine products in lower
dosage counts. While these products
have not been preferred by illicit
methamphetamine manufacturers, they
have nonetheless been subject to
diversion. See, e.g., TNT Distributors, 70
FR 12729, 12730 (2005). Indeed, in light
of recently enacted restrictions on the
sale of List I chemical products imposed
by both Congress and numerous state
legislatures, it is reasonable to expect
that methamphetamine traffickers will
resort to using increasing amounts of
name-brand products.
As I recently explained, ‘‘[b]ecause of
the methamphetamine epidemic’s
devastating effects, DEA has repeatedly
denied an application when an
applicant proposed to sell into the nontraditional market and analysis of one of
the other statutory factors supports the
conclusion that granting the application
would create an unacceptable risk of
diversion.’’ Tri-County Bait, 71 FR at
52164. Thus, even though Respondent
proposes to distribute only name-brand
pseudoephedrine products, the fact that
its proposed customers are primarily
non-traditional retailers (and also
include individuals with no known
business affiliation) and that it has no
effective measures to identify its
customers and determine whether their
purchases would be to meet legitimate
consumer demand, creates an
unacceptable risk that its products
would be diverted. Therefore, while I
acknowledge that none of Respondent’s
officers or employees has a record of
criminal convictions (factor three) and
that the investigative file does not
otherwise establish that Respondent
would fail to comply with applicable
laws (factor two), I conclude that
granting Respondent’s application
would be inconsistent with the public
interest. See Joy’s Ideas, 70 FR at 33199
(registrant’s ‘‘lack of a criminal record,
previous general compliance with the
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law and regulations and willingness to
comply with regulations and guard
against diversion, are far outweighed by
[registrant’s] intent to continue selling
* * * pseudoephedrine exclusively in
the gray market’’).
Order
Accordingly, pursuant to the
authority vested in me by 21 U.S.C.
823(h), and 28 CFR 0.100(b) and 0.104,
I hereby order that the application of
Integrity Wholesale, Inc., for a DEA
Certificate of Registration as a
distributor of List I chemicals be, and it
hereby is, denied. This order is effective
November 13, 2006.
Dated: September 29, 2006.
Michele M. Leonhart,
Deputy Administrator.
[FR Doc. E6–16757 Filed 10–10–06; 8:45 am]
BILLING CODE 4410–09–P
DEPARTMENT OF JUSTICE
Drug Enforcement Administration
Premier Holdings, Inc.; Denial of
Application
On October 20, 2005, the Acting
Deputy Assistant Administrator, Office
of Diversion Control, Drug Enforcement
Administration, issued an Order to
Show Cause to Premier Holdings, Inc.
(Respondent), d/b/a/ Filmart, of
Brooklyn, New York. The Show Cause
Order proposed to deny Respondent’s
application for a DEA Certificate of
Registration as a distributor of List I
chemicals, on the ground that issuance
of a registration would be inconsistent
with the public interest. See 21 U.S.C.
823(h); Show Cause Order at 1.
The Show Cause Order specifically
alleged that Respondent was proposing
to distribute List I chemical products
containing pseudoephedrine to various
firms including convenience stores. See
Show Cause Order at 3. The Show
Cause Order alleged that DEA has
determined that convenience stores
constitute a non-traditional or ‘‘gray
market’’ for products containing
pseudoephedrine and that there is ‘‘a
high incidence of diversion’’ of these
products from these retailers into the
illicit manufacture of
methamphetamine, a Schedule II
controlled substance. Id. at 2. The Show
Cause Order also alleged that even
traditional cold and cough products
have been diverted into the illicit
manufacture of methamphetamine. Id.
at 2.
The Show Cause Order further alleged
that Respondent’s owner, Mr. Eugene
Lefkowitz, told DEA investigators that
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his firm, which sells film, phone cards,
batteries, and health and beauty
products, was seeking registration
because it was ‘‘losing business.’’ Id. at
3. The Show Cause Order alleged that
Mr. Lefkowitz estimated that his sales of
List I chemicals products would amount
to approximately 10 percent of his
firm’s total annual sales of $25 million.
See id.
The Show Cause Order also alleged
that Mr. Lefkowitz provided
investigators with a list of potential
suppliers and a list of products which
Respondent intended to distribute. See
id. The Show Cause Order alleged that
while the product list included
‘‘predominately traditional
pseudoephedrine products * * *. these
products were not consistent with the
known product lines of several
suppliers.’’ See id.
The Show Cause Order alleged that
Respondent provided the investigators
with a list of 25 prospective customers
for List I chemicals of which only 2
were located in New York State. Id. at
3. The Show Cause Order alleged that
investigators conducted verifications
with 17 of the prospective customers,
and that while all of the customers
acknowledged having bought film from
Respondent, 15 of them informed the
investigators ‘‘that they had never
discussed purchasing listed chemical
products from’’ Respondent. Id.
The Show Cause Order further alleged
that many of these customers were large
distributors who were ‘‘capable of
purchasing products directly from the
manufacturers.’’ Id. The Show Cause
Order also alleged that Mr. Lefkowitz
subsequently claimed to investigators
that he was ‘‘losing money’’ because his
customers were requesting that he sell
them List I chemical products and
lacked a registration to do so. Id.
Finally, the Show Cause Order alleged
that Respondent ‘‘and its principals
* * * failed to provide truthful and
accurate information about the nature of
their business * * * and cannot be
expected to properly discharge the
duties of a registrant.’’ Id.
The Show Cause Order was sent by
certified mail to Respondent’s business
address as listed on its application.
According to United States Postal
Service records, Respondent received
the Show Cause Order on October 31,
2005.
Since the effectuation of service,
neither Respondent, nor anyone
purporting to represent it, has
responded. Because (1) more than 30
days have passed since Respondent
received the Show Cause Order, and (2)
no request for a hearing has been
received, I conclude that Respondent
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has waived its right to a hearing. See 21
CFR 1309.53(c). I therefore enter this
final order without a hearing based on
relevant material contained in the
investigative file and make the
following findings.
Findings
Pseudoephedrine is a List I chemical
that, while having therapeutic uses, can
be extracted from lawful nonprescription products and used to
manufacture methamphetamine, a
schedule II controlled substance. See 21
U.S.C. 802(34); 21 CFR 1308.12(d). As
noted in numerous prior DEA orders,
‘‘methamphetamine is an extremely
potent central nervous system
stimulant.’’ Sujak Distributors, 71 FR
50102, 50103 (2006); A–1 Distribution
Wholesale, 70 FR 28573 (2005).
Methamphetamine abuse has destroyed
lives and families, ravaged
communities, and caused serious
environmental harms. Sujak, 71 FR at
50103.
Respondent is a corporation which is
located at 4111 Glenwood Road,
Brooklyn, New York. On June 8, 2004,
Respondent submitted an application
for a Certificate of Registration to
distribute pseudoephedrine.
On October 19, 2004, two DEA
Diversion Investigators (DIs) visited
Respondent at its proposed registered
location to conduct a pre-registration
investigation. The DIs met with Mr.
Eugene Lefkowitz, Respondent’s
President, and Mr. Aron Kohn, its
General Manager. The DIs presented
their credentials, discussed the nature of
their visit, inspected the facility and
interviewed Mssrs. Lefkowitz and Kohn
regarding the firm’s business.
Respondent is located in an industrial
area of Brooklyn and occupies a
warehouse built of brick and
cinderblock. According to the
investigative file, the warehouse has
motion detectors, cameras, and an alarm
system. All visitors are screened and
warehouse access is limited to certain
employees. The List I chemicals would
be stored on shelves located near the
warehouse manager’s desk. The
investigative file indicates that only four
employees would have access to List I
chemicals. Moreover, the investigation
did not uncover any adverse
information as to any of these
employees or the firm’s officers. Finally,
Respondent’s recordkeeping practices
apparently would comply with DEA
regulations.
During the interview, the DIs were
informed that Respondent had total
annual sales of approximately $25
million and that the firm had been in
business for approximately 10 years.
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Respondent sells film, batteries, and
health and beauty products to drug
stores, supermarkets, wholesalers, and
convenience stores throughout the
United States.
Most significantly, Respondent had
no experience in distributing List I
chemicals. Mssrs. Kohn and Lefkowitz
told the DIs that the firm intended to
distribute name brand, over-the-counter,
cold and flu medications containing
pseudoephedrine. Mssrs. Kohn and
Lefkowitz also stated to the DIs that
their customers frequently requested
name brand cold and flu remedies.
Mr. Kohn provided the DIs with a list
of the products Respondent intended to
distribute. The List contained only
traditional name brand products. Mr.
Kohn also provided the DIs with a list
of suppliers. Several of the firms were,
however, under investigation for
supplying products that have been
diverted into the illicit manufacture of
methamphetamine.
Mr. Kohn also provided the DIs with
a list of twenty-five potential customers.
All but two of these customers were
located outside of New York State. The
customer list included large grocery and
drug store chains, as well as large
wholesalers who supply grocery and
drug store chains and convenience
stores.1 Most of the firms already had
DEA registrations authorizing them to
distribute List I chemicals.
Thereafter, a DI contacted five of the
firms. Three of the firms told the DI that
they were no longer buying products
from Respondent.
On March 23, 2005, Mr. Lefkowitz
called Ms. Margaret Brophy, the
Diversion Program Manager for the New
York Field Division to inquire about the
status of his application. During the
conversation, Mr. Lefkowitz related that
1 The customer list included Winn Dixie Stores,
Inc., which owns approximately 920 grocery and
drug stores in the southeastern U.S.; Wakefern Food
Corp., a cooperative of independent grocers who
operate more than 200 Shop Rite Supermarkets
(more than half of which have pharmacies)
throughout the northeastern U.S.; and Brookshire
Grocery, which operates more than 150 stores in
Texas and adjacent states. The list also included
USA Drugs, which distributes health and beauty
products to more than 1,000 grocery, drug, and
discount stores, and which operates more than 170
drug stores in Arkansas and adjacent states; and
Discount Drug Mart, Inc., which operates more than
60 stores in Ohio. The list further included EbyBrown Co., the largest privately owned wholesale
distributor of various products to convenience
stores in the U.S. with more than 25,000 customers
in the midwestern and southeastern U.S.; Spartan
Stores, which owns and operates 68 supermarkets
and 19 drugstores in Michigan and Ohio, and which
also distributes products to more than 350
independent grocery stores in the midwestern U.S.;
and Grocery Supply Co., which supplies more than
15,000 independently-owned supermarkets,
convenience stores, wholesale houses, discount
stores and other retailers.
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he was losing business because he could
not fully service his customers by
selling them pseudoephedrine products
and that his customers had told him that
if his firm could not provide them with
all the items they required, they would
take their business to a firm that would.
Mr. Lefkowitz further claimed that he
was being forced to offer deep discounts
to maintain his customer base.
Ms. Brophy asked Mr. Lefkowitz why
most of Respondent’s customers were
located outside of New York. Mr.
Lefkowitz stated that he had lost New
York customers because his firm could
not supply them with all the products
they required. Mr. Lefkowitz further
related that his non-New York based
customers were less demanding with
respect to purchasing all of their
products from one source.
Thereafter, in May 2005, a DI
conducted additional inquiries of the
firms listed on Respondent’s customer
list and contacted seventeen of the
firms. While all of the firms verified that
they had purchased film from
Respondent, fifteen of the firms
informed the DI that they had never
discussed with Respondent the
purchase of List I chemical products
from it.2
Discussion
Under 21 U.S.C. 823(h), an applicant
to distribute List I chemicals is entitled
to be registered unless I determine that
the registration would be ‘‘inconsistent
with the public interest.’’ In making this
determination, Congress directed that I
consider the following factors:
(1) Maintenance by the applicant 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. ‘‘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 an
application for registration should be
denied. See, e.g., David M. Starr, 71 FR
2 Two of the firms had discussed purchasing List
I chemicals from Respondent.
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39367, 39368 (2006); Energy Outlet, 64
FR 14269, 14271 (1999). In this case, I
conclude that factors four and five are
dispositive and establish that
Respondent’s application should be
denied.
Factor One—Maintenance of Effective
Controls Against Diversion
The investigative file does not
establish that Respondent would fail to
maintain effective controls against the
theft and diversion of listed chemicals.
Respondent’s facility appears to meet
DEA’s regulations pertaining to physical
security. See 21 CFR 1309.71(b)(1)–(7).
Moreover, it appears that Respondent
has an adequate system ‘‘for monitoring
the receipt, distribution, and disposition
of List I chemicals.’’ Id. § 1309.71(b)(8).
I thus conclude that this factor supports
a finding that Respondent’s registration
would be consistent with the public
interest.
Factors Two and Three—Compliance
With Applicable Law and the
Applicant’s Prior Record of Relevant
Criminal Convictions
The investigative file does not
establish that Respondent has failed to
comply with applicable Federal, State,
and local laws. Moreover, there is no
evidence establishing that Respondent,
any of its officers, or any employee with
access to List I chemicals has been
convicted of a criminal offense related
to controlled substances or chemicals.
Both factors thus support a finding that
Respondent’s registration would be
consistent with the public interest.
Factor Four—The Applicant’s Past
Experience In Distributing Chemicals
The investigative file establishes that
Respondent has no experience
distributing List I chemicals. Moreover,
Respondent did not provide evidence to
the DIs that any of its employees have
experience in distributing List I
chemicals. Because of the high risk of
diversion, DEA has repeatedly held that
an applicant’s (and its employees’) lack
of experience in distributing List I
chemicals is a factor that weighs heavily
against granting an application for a
registration. Sujak Distributors, 71 FR at
50104; Jay Enterprises, 70 FR 24620,
24621 (2005); ANM Wholesale, 69 FR
11652, 11653 (2004). This factor thus
supports a finding that Respondent’s
registration would be inconsistent with
the public interest.
Factor Five—Other Factors That Are
Relevant To and Consistent With Public
Health and Safety
Numerous DEA cases recognize that
the sale of List I chemical products by
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non-traditional retailers such as
convenience stores is an area of
particular concern in preventing
diversion of these products into the
illicit manufacture of
methamphetamine. See, e.g., Joey
Enterprises, 70 FR 76866, 76867 (2005).
As Joey Enterprises explains, ‘‘[w]hile
there are no specific prohibitions under
the Controlled Substances Act regarding
the sale of listed chemical products to
[convenience stores], DEA has
nevertheless found that [these entities]
constitute sources for the diversion of
listed chemical products.’’ Id. See also
TNT Distributors, 70 FR 12729, 12730
(2005) (special agent testified that ‘‘80 to
90 percent of ephedrine and
pseudoephedrine being used [in
Tennessee] to manufacture
methamphetamine was being obtained
from convenience stores’’); OTC
Distribution Co., 68 FR 70538, 70541
(2003) (noting ‘‘over 20 different
seizures of [gray market distributor’s]
pseudoephedrine product at clandestine
sites,’’ and that in an eight month period
distributor’s product ‘‘was seized at
clandestine laboratories in eight states,
with over 2 million dosage units seized
in Oklahoma alone.’’); MDI
Pharmaceuticals, 68 FR 4233, 4236
(2003) (finding that ‘‘pseudoephedrine
products distributed by [gray market
distributor] have been uncovered at
numerous clandestine
methamphetamine settings throughout
the United States and/or discovered in
the possession of individuals apparently
involved in the illicit manufacture of
methamphetamine’’).
Respondent’s list of potential
customers included wholesale
distributors to convenience stores.
Moreover, during the on-site inspection,
the DIs determined that Respondent
sells various products to convenience
stores. DEA final orders recognize that
there is a substantial risk of diversion of
List I chemicals into the illicit
manufacture of methamphetamine when
these products are sold by these nontraditional retailers. See, e.g., Joy’s
Ideas, 70 FR at 33199 (finding that the
risk of diversion was ‘‘real, substantial
and compelling’’); Jay Enterprises, 70 FR
at 24621 (noting ‘‘heightened risk of
diversion’’ should application be
granted).
I acknowledge that Respondent’s list
of potential customers included grocery
chains, drug store chains, and wholesale
distributors to these firms. DEA has
found that these firms constitute the
traditional market for pseudoephedrine
products. See, e.g., D & S Sales, 71 FR
37607, 37608–09 (2006); Joy’s Ideas, 70
FR at 33196–97.
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There is, however, substantial reason
to question the validity of the customer
information Respondent provided to
DEA. In DEA’s experience, many of the
firms listed as potential customers are of
large enough size that they are able to
purchase List I chemical products either
directly from manufacturers or from
large wholesalers. See John Vanags, 71
FR 39365, 39366 (2006). Indeed, it
seems unlikely that Respondent could
offer prices that are competitive with
those offered by the manufacturers of
List I products or large wholesalers.
Most significantly, the investigative
file establishes that Mr. Lefkowitz
represented to DEA investigators that
Respondent’s customers had requested
List I chemical products from his firm
and that he had lost business and was
forced to offer deep discounts to keep
other customers. Yet all but two of the
firms contacted by the DI told her that
they had never discussed the purchase
of List I products with Respondent.
Moreover, several of the firms told the
DI that they were no longer purchasing
products from Respondent.
That the overwhelming majority of
the customers told the DI that they had
never discussed purchasing List I
products from Respondent (and that
some of the firms no longer bought any
products from it) raises a serious
question as to the validity of Mr.
Lefkowitz’s statements to DEA
personnel. Indeed, the information
uncovered by the customer verifications
suggests that Respondent may have
provided the customer list (which
contains legitimate businesses) to
induce DEA to grant it a registration,
which it would then use to distribute
List I products into the non-traditional
market, the principle supply source of
mom-and-pop methamphetamine labs.
Whether this was the intent of
Respondent’s officers I need not decide
because DEA will not grant any
application when there is reason to
question the validity of the information
an applicant has provided.
As it is, it is indisputable that
Respondent’s customers include
convenience stores. Under DEA
precedents, an applicant’s proposal to
sell List I products into the nontraditional market weighs heavily
against the granting of a registration
under factor five. So too here.
DEA has repeatedly denied an
application when an applicant proposed
to sell into the non-traditional market
and the analysis of one of the other
statutory factors supports the
conclusion that granting the application
would create an unacceptable risk of
diversion. Thus, in Xtreme Enterprises,
67 FR 76195, 76197 (2002), my
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16:53 Oct 10, 2006
Jkt 211001
predecessor denied an application,
observing that the respondent’s ‘‘lack of
criminal record, compliance with the
law and willingness to upgrade her
security system are far outweighed by
her lack of experience with selling List
I chemicals and the fact that she intends
to sell ephedrine almost exclusively in
the gray market.’’
More recently, I denied an
application, observing that the
respondent’s ‘‘lack of a criminal record
and any intent to comply with the law
and regulations are far outweighed by
his lack of experience and the
company’s intent to sell ephedrine and
pseudoephedrine exclusively to the gray
market.’’ Jay Enterprises, 70 FR at
24621. Accord Prachi Enterprises, 69 FR
69407, 69409 (2004). Consistent with
these precedents, and considering the
serious concern raised by the
investigation as to Respondent’s
intended customers, I conclude that
granting Respondent’s application for a
registration would be inconsistent with
the public interest.
Order
Accordingly, pursuant to the
authority vested in me by 21 U.S.C.
823(h), as well as 28 CFR 0.100(b) and
0.104, I hereby order that the
application of Premier Holdings, Inc.,
d/b/a/ Filmart, for a DEA Certificate of
Registration as a distributor of List I
chemicals be, and it hereby is, denied.
This order is effective November 13,
2006.
Dated: September 29, 2006.
Michele M. Leonhart,
Deputy Administrator.
[FR Doc. E6–16756 Filed 10–10–06; 8:45 am]
BILLING CODE 4410–09–P
NATIONAL ARCHIVES AND RECORDS
ADMINISTRATION
Information Security Oversight Office
Public Interest Declassification Board
(PIDB); Notice of Meeting
Pursuant to Section 1102 of the
Intelligence Reform and Terrorism
Prevention Act of 2004 which extended
and modified the Public Interest
Declassification Board (PIDB) as
established by the Public Interest
Declassification Act of 2000 (Pub. L.
106–567, title VII, December 27, 2000,
114 Stat. 2856), announcement is made
for the following committee meeting:
Name of Committee: Public Interest
Declassification Board (PIDB).
Date of Meeting: Friday, October 13, 2006.
Time of Meeting: 9 a.m. to 12:30 p.m.
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59837
Place of Meeting: National Archives and
Records Administration, 700 Pennsylvania
Avenue, NW., Archivist’s Reception Room,
Room 105, Washington, DC 20408.
Purpose: To discuss declassification
program issues.
This meeting will be open to the public.
However, due to space limitations and access
procedures, the name and telephone number
of individuals planning to attend must be
submitted to the Information Security
Oversight Office (ISOO) no later than
Wednesday, October 11, 2006. ISOO will
provide additional instructions for gaining
access to the location of the meeting.
For Further Inforamtion Contact: J.
William Leonard, Director Information
Security Oversight Office, National
Archives Building, 700 Pennsylvania
Avenue, NW., Washington, DC 20408,
telephone number (202) 357–5250.
Dated: October 4, 2006.
J. William Leonard,
Director, Information Security Oversight
Office.
[FR Doc. E6–16749 Filed 10–10–06; 8:45 am]
BILLING CODE 7515–01–P
NATIONAL COUNCIL ON DISABILITY
Cultural Diversity Advisory Committee
Meetings (Teleconferences)
Times and Dates:
November 16, 2006, 3 p.m. Eastern.
February 16, 2007, 3 p.m. Eastern.
May 17, 2007, 3 p.m. Eastern.
July 19, 2007, 3 p.m. Eastern.
September 20, 2007, 3 p.m. Eastern.
Place: NCD, 1331 F Street, NW., Suite
850, Washington, DC.
AGENCY: NCD.
Status: All parts of these conference
calls will be open to the public for
observation only. Those interested in
observing on conference calls should
contact the appropriate staff member
listed below. Due to limited resources,
only a few telephone lines will be
available for each conference call.
Agenda: Roll call, announcements,
reports, new business, adjournment.
FOR FURTHER INFORMATION CONTACT:
Gerrie Drake Hawkins, Ph.D., Senior
Program Analyst, NCD, 1331 F Street,
NW., Suite 850, Washington, DC 20004;
202–272–2004 (voice), 202–272–2074
(TTY), 202–272–2022 (fax),
cultural-diversity@ncd.gov (e-mail).
Cultural Diversity Advisory
Committee Mission: The purpose of
NCD’s Cultural Diversity Advisory
Committee is to provide advice and
recommendations to NCD on issues
affecting people with disabilities from
culturally diverse backgrounds.
Specifically, the committee will help
identify issues, expand outreach, infuse
participation, and elevate the voices of
E:\FR\FM\11OCN1.SGM
11OCN1
Agencies
[Federal Register Volume 71, Number 196 (Wednesday, October 11, 2006)]
[Notices]
[Pages 59834-59837]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E6-16756]
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DEPARTMENT OF JUSTICE
Drug Enforcement Administration
Premier Holdings, Inc.; Denial of Application
On October 20, 2005, the Acting Deputy Assistant Administrator,
Office of Diversion Control, Drug Enforcement Administration, issued an
Order to Show Cause to Premier Holdings, Inc. (Respondent), d/b/a/
Filmart, of Brooklyn, New York. The Show Cause Order proposed to deny
Respondent's application for a DEA Certificate of Registration as a
distributor of List I chemicals, on the ground that issuance of a
registration would be inconsistent with the public interest. See 21
U.S.C. 823(h); Show Cause Order at 1.
The Show Cause Order specifically alleged that Respondent was
proposing to distribute List I chemical products containing
pseudoephedrine to various firms including convenience stores. See Show
Cause Order at 3. The Show Cause Order alleged that DEA has determined
that convenience stores constitute a non-traditional or ``gray market''
for products containing pseudoephedrine and that there is ``a high
incidence of diversion'' of these products from these retailers into
the illicit manufacture of methamphetamine, a Schedule II controlled
substance. Id. at 2. The Show Cause Order also alleged that even
traditional cold and cough products have been diverted into the illicit
manufacture of methamphetamine. Id. at 2.
The Show Cause Order further alleged that Respondent's owner, Mr.
Eugene Lefkowitz, told DEA investigators that
[[Page 59835]]
his firm, which sells film, phone cards, batteries, and health and
beauty products, was seeking registration because it was ``losing
business.'' Id. at 3. The Show Cause Order alleged that Mr. Lefkowitz
estimated that his sales of List I chemicals products would amount to
approximately 10 percent of his firm's total annual sales of $25
million. See id.
The Show Cause Order also alleged that Mr. Lefkowitz provided
investigators with a list of potential suppliers and a list of products
which Respondent intended to distribute. See id. The Show Cause Order
alleged that while the product list included ``predominately
traditional pseudoephedrine products * * *. these products were not
consistent with the known product lines of several suppliers.'' See id.
The Show Cause Order alleged that Respondent provided the
investigators with a list of 25 prospective customers for List I
chemicals of which only 2 were located in New York State. Id. at 3. The
Show Cause Order alleged that investigators conducted verifications
with 17 of the prospective customers, and that while all of the
customers acknowledged having bought film from Respondent, 15 of them
informed the investigators ``that they had never discussed purchasing
listed chemical products from'' Respondent. Id.
The Show Cause Order further alleged that many of these customers
were large distributors who were ``capable of purchasing products
directly from the manufacturers.'' Id. The Show Cause Order also
alleged that Mr. Lefkowitz subsequently claimed to investigators that
he was ``losing money'' because his customers were requesting that he
sell them List I chemical products and lacked a registration to do so.
Id. Finally, the Show Cause Order alleged that Respondent ``and its
principals * * * failed to provide truthful and accurate information
about the nature of their business * * * and cannot be expected to
properly discharge the duties of a registrant.'' Id.
The Show Cause Order was sent by certified mail to Respondent's
business address as listed on its application. According to United
States Postal Service records, Respondent received the Show Cause Order
on October 31, 2005.
Since the effectuation of service, neither Respondent, nor anyone
purporting to represent it, has responded. Because (1) more than 30
days have passed since Respondent received the Show Cause Order, and
(2) no request for a hearing has been received, I conclude that
Respondent has waived its right to a hearing. See 21 CFR 1309.53(c). I
therefore enter this final order without a hearing based on relevant
material contained in the investigative file and make the following
findings.
Findings
Pseudoephedrine is a List I chemical that, while having therapeutic
uses, can be extracted from lawful non-prescription products and used
to manufacture methamphetamine, a schedule II controlled substance. See
21 U.S.C. 802(34); 21 CFR 1308.12(d). As noted in numerous prior DEA
orders, ``methamphetamine is an extremely potent central nervous system
stimulant.'' Sujak Distributors, 71 FR 50102, 50103 (2006); A-1
Distribution Wholesale, 70 FR 28573 (2005). Methamphetamine abuse has
destroyed lives and families, ravaged communities, and caused serious
environmental harms. Sujak, 71 FR at 50103.
Respondent is a corporation which is located at 4111 Glenwood Road,
Brooklyn, New York. On June 8, 2004, Respondent submitted an
application for a Certificate of Registration to distribute
pseudoephedrine.
On October 19, 2004, two DEA Diversion Investigators (DIs) visited
Respondent at its proposed registered location to conduct a pre-
registration investigation. The DIs met with Mr. Eugene Lefkowitz,
Respondent's President, and Mr. Aron Kohn, its General Manager. The DIs
presented their credentials, discussed the nature of their visit,
inspected the facility and interviewed Mssrs. Lefkowitz and Kohn
regarding the firm's business.
Respondent is located in an industrial area of Brooklyn and
occupies a warehouse built of brick and cinderblock. According to the
investigative file, the warehouse has motion detectors, cameras, and an
alarm system. All visitors are screened and warehouse access is limited
to certain employees. The List I chemicals would be stored on shelves
located near the warehouse manager's desk. The investigative file
indicates that only four employees would have access to List I
chemicals. Moreover, the investigation did not uncover any adverse
information as to any of these employees or the firm's officers.
Finally, Respondent's recordkeeping practices apparently would comply
with DEA regulations.
During the interview, the DIs were informed that Respondent had
total annual sales of approximately $25 million and that the firm had
been in business for approximately 10 years. Respondent sells film,
batteries, and health and beauty products to drug stores, supermarkets,
wholesalers, and convenience stores throughout the United States.
Most significantly, Respondent had no experience in distributing
List I chemicals. Mssrs. Kohn and Lefkowitz told the DIs that the firm
intended to distribute name brand, over-the-counter, cold and flu
medications containing pseudoephedrine. Mssrs. Kohn and Lefkowitz also
stated to the DIs that their customers frequently requested name brand
cold and flu remedies.
Mr. Kohn provided the DIs with a list of the products Respondent
intended to distribute. The List contained only traditional name brand
products. Mr. Kohn also provided the DIs with a list of suppliers.
Several of the firms were, however, under investigation for supplying
products that have been diverted into the illicit manufacture of
methamphetamine.
Mr. Kohn also provided the DIs with a list of twenty-five potential
customers. All but two of these customers were located outside of New
York State. The customer list included large grocery and drug store
chains, as well as large wholesalers who supply grocery and drug store
chains and convenience stores.\1\ Most of the firms already had DEA
registrations authorizing them to distribute List I chemicals.
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\1\ The customer list included Winn Dixie Stores, Inc., which
owns approximately 920 grocery and drug stores in the southeastern
U.S.; Wakefern Food Corp., a cooperative of independent grocers who
operate more than 200 Shop Rite Supermarkets (more than half of
which have pharmacies) throughout the northeastern U.S.; and
Brookshire Grocery, which operates more than 150 stores in Texas and
adjacent states. The list also included USA Drugs, which distributes
health and beauty products to more than 1,000 grocery, drug, and
discount stores, and which operates more than 170 drug stores in
Arkansas and adjacent states; and Discount Drug Mart, Inc., which
operates more than 60 stores in Ohio. The list further included Eby-
Brown Co., the largest privately owned wholesale distributor of
various products to convenience stores in the U.S. with more than
25,000 customers in the midwestern and southeastern U.S.; Spartan
Stores, which owns and operates 68 supermarkets and 19 drugstores in
Michigan and Ohio, and which also distributes products to more than
350 independent grocery stores in the midwestern U.S.; and Grocery
Supply Co., which supplies more than 15,000 independently-owned
supermarkets, convenience stores, wholesale houses, discount stores
and other retailers.
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Thereafter, a DI contacted five of the firms. Three of the firms
told the DI that they were no longer buying products from Respondent.
On March 23, 2005, Mr. Lefkowitz called Ms. Margaret Brophy, the
Diversion Program Manager for the New York Field Division to inquire
about the status of his application. During the conversation, Mr.
Lefkowitz related that
[[Page 59836]]
he was losing business because he could not fully service his customers
by selling them pseudoephedrine products and that his customers had
told him that if his firm could not provide them with all the items
they required, they would take their business to a firm that would. Mr.
Lefkowitz further claimed that he was being forced to offer deep
discounts to maintain his customer base.
Ms. Brophy asked Mr. Lefkowitz why most of Respondent's customers
were located outside of New York. Mr. Lefkowitz stated that he had lost
New York customers because his firm could not supply them with all the
products they required. Mr. Lefkowitz further related that his non-New
York based customers were less demanding with respect to purchasing all
of their products from one source.
Thereafter, in May 2005, a DI conducted additional inquiries of the
firms listed on Respondent's customer list and contacted seventeen of
the firms. While all of the firms verified that they had purchased film
from Respondent, fifteen of the firms informed the DI that they had
never discussed with Respondent the purchase of List I chemical
products from it.\2\
---------------------------------------------------------------------------
\2\ Two of the firms had discussed purchasing List I chemicals
from Respondent.
---------------------------------------------------------------------------
Discussion
Under 21 U.S.C. 823(h), an applicant to distribute List I chemicals
is entitled to be registered unless I determine that the registration
would be ``inconsistent with the public interest.'' In making this
determination, Congress directed that I consider the following factors:
(1) Maintenance by the applicant 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. ``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 an application for registration should be denied.
See, e.g., David M. Starr, 71 FR 39367, 39368 (2006); Energy Outlet, 64
FR 14269, 14271 (1999). In this case, I conclude that factors four and
five are dispositive and establish that Respondent's application should
be denied.
Factor One--Maintenance of Effective Controls Against Diversion
The investigative file does not establish that Respondent would
fail to maintain effective controls against the theft and diversion of
listed chemicals. Respondent's facility appears to meet DEA's
regulations pertaining to physical security. See 21 CFR 1309.71(b)(1)-
(7). Moreover, it appears that Respondent has an adequate system ``for
monitoring the receipt, distribution, and disposition of List I
chemicals.'' Id. Sec. 1309.71(b)(8). I thus conclude that this factor
supports a finding that Respondent's registration would be consistent
with the public interest.
Factors Two and Three--Compliance With Applicable Law and the
Applicant's Prior Record of Relevant Criminal Convictions
The investigative file does not establish that Respondent has
failed to comply with applicable Federal, State, and local laws.
Moreover, there is no evidence establishing that Respondent, any of its
officers, or any employee with access to List I chemicals has been
convicted of a criminal offense related to controlled substances or
chemicals. Both factors thus support a finding that Respondent's
registration would be consistent with the public interest.
Factor Four--The Applicant's Past Experience In Distributing Chemicals
The investigative file establishes that Respondent has no
experience distributing List I chemicals. Moreover, Respondent did not
provide evidence to the DIs that any of its employees have experience
in distributing List I chemicals. Because of the high risk of
diversion, DEA has repeatedly held that an applicant's (and its
employees') lack of experience in distributing List I chemicals is a
factor that weighs heavily against granting an application for a
registration. Sujak Distributors, 71 FR at 50104; Jay Enterprises, 70
FR 24620, 24621 (2005); ANM Wholesale, 69 FR 11652, 11653 (2004). This
factor thus supports a finding that Respondent's registration would be
inconsistent with the public interest.
Factor Five--Other Factors That Are Relevant To and Consistent With
Public Health and Safety
Numerous DEA cases recognize that the sale of List I chemical
products by non-traditional retailers such as convenience stores is an
area of particular concern in preventing diversion of these products
into the illicit manufacture of methamphetamine. See, e.g., Joey
Enterprises, 70 FR 76866, 76867 (2005). As Joey Enterprises explains,
``[w]hile there are no specific prohibitions under the Controlled
Substances Act regarding the sale of listed chemical products to
[convenience stores], DEA has nevertheless found that [these entities]
constitute sources for the diversion of listed chemical products.'' Id.
See also TNT Distributors, 70 FR 12729, 12730 (2005) (special agent
testified that ``80 to 90 percent of ephedrine and pseudoephedrine
being used [in Tennessee] to manufacture methamphetamine was being
obtained from convenience stores''); OTC Distribution Co., 68 FR 70538,
70541 (2003) (noting ``over 20 different seizures of [gray market
distributor's] pseudoephedrine product at clandestine sites,'' and that
in an eight month period distributor's product ``was seized at
clandestine laboratories in eight states, with over 2 million dosage
units seized in Oklahoma alone.''); MDI Pharmaceuticals, 68 FR 4233,
4236 (2003) (finding that ``pseudoephedrine products distributed by
[gray market distributor] have been uncovered at numerous clandestine
methamphetamine settings throughout the United States and/or discovered
in the possession of individuals apparently involved in the illicit
manufacture of methamphetamine'').
Respondent's list of potential customers included wholesale
distributors to convenience stores. Moreover, during the on-site
inspection, the DIs determined that Respondent sells various products
to convenience stores. DEA final orders recognize that there is a
substantial risk of diversion of List I chemicals into the illicit
manufacture of methamphetamine when these products are sold by these
non-traditional retailers. See, e.g., Joy's Ideas, 70 FR at 33199
(finding that the risk of diversion was ``real, substantial and
compelling''); Jay Enterprises, 70 FR at 24621 (noting ``heightened
risk of diversion'' should application be granted).
I acknowledge that Respondent's list of potential customers
included grocery chains, drug store chains, and wholesale distributors
to these firms. DEA has found that these firms constitute the
traditional market for pseudoephedrine products. See, e.g., D & S
Sales, 71 FR 37607, 37608-09 (2006); Joy's Ideas, 70 FR at 33196-97.
[[Page 59837]]
There is, however, substantial reason to question the validity of
the customer information Respondent provided to DEA. In DEA's
experience, many of the firms listed as potential customers are of
large enough size that they are able to purchase List I chemical
products either directly from manufacturers or from large wholesalers.
See John Vanags, 71 FR 39365, 39366 (2006). Indeed, it seems unlikely
that Respondent could offer prices that are competitive with those
offered by the manufacturers of List I products or large wholesalers.
Most significantly, the investigative file establishes that Mr.
Lefkowitz represented to DEA investigators that Respondent's customers
had requested List I chemical products from his firm and that he had
lost business and was forced to offer deep discounts to keep other
customers. Yet all but two of the firms contacted by the DI told her
that they had never discussed the purchase of List I products with
Respondent. Moreover, several of the firms told the DI that they were
no longer purchasing products from Respondent.
That the overwhelming majority of the customers told the DI that
they had never discussed purchasing List I products from Respondent
(and that some of the firms no longer bought any products from it)
raises a serious question as to the validity of Mr. Lefkowitz's
statements to DEA personnel. Indeed, the information uncovered by the
customer verifications suggests that Respondent may have provided the
customer list (which contains legitimate businesses) to induce DEA to
grant it a registration, which it would then use to distribute List I
products into the non-traditional market, the principle supply source
of mom-and-pop methamphetamine labs. Whether this was the intent of
Respondent's officers I need not decide because DEA will not grant any
application when there is reason to question the validity of the
information an applicant has provided.
As it is, it is indisputable that Respondent's customers include
convenience stores. Under DEA precedents, an applicant's proposal to
sell List I products into the non-traditional market weighs heavily
against the granting of a registration under factor five. So too here.
DEA has repeatedly denied an application when an applicant proposed
to sell into the non-traditional market and the analysis of one of the
other statutory factors supports the conclusion that granting the
application would create an unacceptable risk of diversion. Thus, in
Xtreme Enterprises, 67 FR 76195, 76197 (2002), my predecessor denied an
application, observing that the respondent's ``lack of criminal record,
compliance with the law and willingness to upgrade her security system
are far outweighed by her lack of experience with selling List I
chemicals and the fact that she intends to sell ephedrine almost
exclusively in the gray market.''
More recently, I denied an application, observing that the
respondent's ``lack of a criminal record and any intent to comply with
the law and regulations are far outweighed by his lack of experience
and the company's intent to sell ephedrine and pseudoephedrine
exclusively to the gray market.'' Jay Enterprises, 70 FR at 24621.
Accord Prachi Enterprises, 69 FR 69407, 69409 (2004). Consistent with
these precedents, and considering the serious concern raised by the
investigation as to Respondent's intended customers, I conclude that
granting Respondent's application for a registration would be
inconsistent with the public interest.
Order
Accordingly, pursuant to the authority vested in me by 21 U.S.C.
823(h), as well as 28 CFR 0.100(b) and 0.104, I hereby order that the
application of Premier Holdings, Inc., d/b/a/ Filmart, for a DEA
Certificate of Registration as a distributor of List I chemicals be,
and it hereby is, denied. This order is effective November 13, 2006.
Dated: September 29, 2006.
Michele M. Leonhart,
Deputy Administrator.
[FR Doc. E6-16756 Filed 10-10-06; 8:45 am]
BILLING CODE 4410-09-P