[Federal Register Volume 67, Number 52 (Monday, March 18, 2002)]
[Notices]
[Page 12049]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 02-6322]


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DEPARTMENT OF JUSTICE

Drug Enforcement Administration


Manufacturer of Controlled Substances; Notice of Registration

    By Notice dated October 2, 2001, and published in the Federal 
Register on October 11, 2001, (66 FR 51970), LifePoint, Inc., 10410 
Trademark Street, Rancho Cucamonga, California 91730, made application 
by renewal to the Drug Enforcement Administration (DEA) to be 
registered as a bulk manufacturer of the basic classes of controlled 
substances listed below:

------------------------------------------------------------------------
                    Drug                               Schedule
------------------------------------------------------------------------
Tetrahydrocannabinols (7370)...............  I
Amphetamine (1100).........................  II
Methamphetamine (1105).....................  II
Phencyclidine (7471).......................  II
Benzoylecgonine (9180).....................  II
Morphine (9300)............................  II
------------------------------------------------------------------------

    The firm plans to use gram quantities of the listed controlled 
substances to manufacture drug abuse test kits.
    No comments or objections have been received. DEA has considered 
the factors in Title 21, United States Code, section 823(a) and 
determined that the registration of LifePoint, Inc. to manufacture the 
listed controlled substances is consistent with the public interest at 
this time. DEA has investigated the firm on a regular basis to ensure 
that the company's continued registration is consistent with the public 
interest. These investigations have included inspection and testing of 
the company's physical security systems, audits of the company's 
records, verification of the company's compliance with State and local 
laws, and a review of the company's background and history. Therefore, 
pursuant to 21 U.S.C. 823 and 28 CFR 0.100 and 0.104, the Deputy 
Assistant Administrator, Office of Diversion Control, hereby orders 
that the application submitted by the above firm for registration as a 
bulk manufacturer of the basic classes of controlled substances listed 
above is granted.

    Dated: March 7, 2002.
Laura M. Nagel,
Deputy Assistant Administrator, Office of Diversion Control, Drug 
Enforcement Administration.
[FR Doc. 02-6322 Filed 3-15-02; 8:45 am]
BILLING CODE 4410-09-M