Guideline for the manufacture of in vitro diagnostic products

Other Authors: Center for Devices and Radiological Health (U.S.). Division of Compliance Programs.
Format: Book
Language: English
Published: Rockville, Md. : Division of Compliance Programs, Office of Compliance and Surveillance, Center for Devices and Radiological Health, Food and Drug Administration, [1990]
Physical Description: 39 pages ; 28 cm.
Subjects:
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245 0 0 |a Guideline for the manufacture of in vitro diagnostic products. 
264 1 |a Rockville, Md. :  |b Division of Compliance Programs, Office of Compliance and Surveillance, Center for Devices and Radiological Health, Food and Drug Administration,  |c [1990] 
300 |a 39 pages ;  |c 28 cm. 
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338 |a volume  |b nc  |2 rdacarrier. 
500 |a "Second draft." 
500 |a Shipping list no.: 90-365-P. 
500 |a "February 1990." 
504 |a Includes bibliographical references (pages 34-36). 
650 0 |a Diagnosis, Laboratory  |x Equipment and supplies  |v Handbooks, manuals, etc. 
650 0 |a Medical instruments and apparatus  |x Standards  |z United States  |v Handbooks, manuals, etc. 
655 7 |a Handbooks and manuals.  |2 lcgft. 
710 2 |a Center for Devices and Radiological Health (U.S.).  |b Division of Compliance Programs. 
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