Guideline for the manufacture of in vitro diagnostic products.

Bibliographic Details
Corporate Author:	Center for Devices and Radiological Health (U.S.). Division of Compliance Programs
Format:	Government Document 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]
Subjects:	Diagnosis, Laboratory > Equipment and supplies > Handbooks, manuals, etc. Medical instruments and apparatus > Standards > United States > Handbooks, manuals, etc.

Evans: US Documents (Annex 5th floor)