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Varian, Inc.
FR Doc E8-18042[Federal Register: August 6, 2008 (Volume 73, Number 152)]
[Notices] [Page 45788-45789] From the Federal Register Online via GPO Access [wais.access.gpo.gov]
[DOCID:fr06au08-105]
DEPARTMENT OF JUSTICE
Drug Enforcement Administration
Manufacturer of Controlled Substances; Notice of Registration
By Notice dated March 11, 2008 and published in the Federal Register on March
19, 2008 (73 FR 14841), Varian, Inc., Lake Forest, 25200 Commercentre Drive,
Lake Forest, California 92630-8810, 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 in schedule II:
Drug
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Schedule
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Phencyclidine (7471)
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II
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1-Piperidinocyclohexane-carbonitrile (8603)
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II
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Benzoylecgonine (9180)
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II
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The company plans to manufacture small quantities of the listed controlled
substances for use in diagnostic products.
No comments or objections have been received. DEA has considered the factors
in 21 U.S.C. 823(a) and determined that the registration of Varian, Inc. to
manufacture the listed
[[Page 45789]]
basic classes of controlled substances is consistent with the public interest
at this time. DEA has investigated Varian, Inc. to ensure that the company's
registration is consistent with the public interest. The investigation has
included inspection and testing of the company's physical security systems,
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 in accordance with 21 CFR
1301.33, the above named company is granted
registration as a bulk manufacturer of the basic classes of controlled
substances listed.
Dated: July 30, 2008.
Joseph T. Rannazzisi,
Deputy Assistant Administrator, Office of Diversion
Control, Drug Enforcement Administration.
[FR Doc. E8-18042 Filed 8-5-08; 8:45 am]
BILLING CODE 4410-09-P
NOTICE: This is an
unofficial version. An official version of these publications may be obtained
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