United States Government Publishing Office
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United States
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2017-01-09
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Viruses, Serums, Toxins, and Analogous Products; Sampling of Biological Products
Part IV
UNKNOWN
D09002ee1be0736b4
United States
Department of Agriculture
originator
org
United States Government Agency or Subagency
United States
Animal and Plant Health Inspection Service
originator
org
United States Government Agency or Subagency
We are proposing to amend the regulations regarding the number of samples that a firm would need to submit to the Animal and Plant Health Inspection Service for testing at the National Veterinary Services Laboratories (NVSL), Ames, Iowa. The effect of the proposed amendment would be to specify the number of samples that NVSL would need for diagnostic test kits and for Master Seeds and Cells. The proposed amendment is necessary to provide criteria to licensees regarding diagnostic test kits and Master Seeds and Cells because no criteria are currently included in the regulations.
59 FR 0
https://www.govinfo.gov/app/details/FR-1994-03-24/94-6947
94-6947
fr24mr94-18
3410-34-P
Federal Register: March 24, 1994
Docket No. 93-057-1
https://www.govinfo.gov/app/details/FR-1994-03-24/94-6947
https://www.govinfo.gov/content/pkg/FR-1994-03-24/html/94-6947.htm
1 p.
0
0
59 FR 0
Code of Federal Regulations
Title 9 Part 113
9 CFR Part 113
Viruses, Serums, Toxins, and Analogous Products; Sampling of Biological Products; Federal Register Vol. 59, Issue
UNKNOWN
94-6947
IV
DEPARTMENT OF AGRICULTURE
Animal and Plant Health Inspection Service
1994-05-23
Federal Register: March 24, 1994
Docket No. 93-057-1
3410-34-P
94-6947
Proposed rule.
We are proposing to amend the regulations regarding the number of samples that a firm would need to submit to the Animal and Plant Health Inspection Service for testing at the National Veterinary Services Laboratories (NVSL), Ames, Iowa. The effect of the proposed amendment would be to specify the number of samples that NVSL would need for diagnostic test kits and for Master Seeds and Cells. The proposed amendment is necessary to provide criteria to licensees regarding diagnostic test kits and Master Seeds and Cells because no criteria are currently included in the regulations.
Consideration will be given only to comments received on or before May 23, 1994.
Dr. Richard E. Pacer, Senior Staff Veterinarian, Veterinary Biologics, BBEP, APHIS, USDA, room 838, Federal Building, 6505 Belcrest Road, Hyattsville, MD 20782, (301) 436- 8245.
Federal Register
Vol. 59, no. 57
Office of the Federal Register, National Archives and Records Administration
1994-03-24
continuing
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236 p.
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