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Guideline for the manufacture of in vitro diagnostic products
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
Additional Creators:
Center for Devices and Radiological Health (U.S.). Division of Compliance Programs
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Report Numbers:
HE 20.4608:In 1/2/draft
Subject(s):
Diagnosis, Laboratory
—
Equipment and supplies
—
Handbooks, manuals, etc
Medical instruments and apparatus
—
Standards
—
United States
—
Handbooks, manuals, etc
Note:
"February 1990".
"Second draft".
Bibliography Note:
Includes bibliographical references (pages 34-36).
View MARC record
| catkey: 573312