Guideline for the manufacture of in vitro diagnostic products.
| Corporate Author: | |
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| 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]
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| Subjects: |
| Item Description: | "Second draft." Shipping list number: 90-365-P. "February 1990." |
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| Physical Description: | 39 pages ; 28 cm. |
| Bibliography: | Includes bibliographical references (pages 34-36). |