HIEMSTRA APPROVED TO MANUFACTURE MEDICAL DEVICES IN CLEAN ROOM. | Biotech Equipment Update (February, 2008)

HIEMSTRA APPROVED TO MANUFACTURE MEDICAL DEVICES IN CLEAN ROOM.
Publication Date: 01-FEB-08
Publication Title: Biotech Equipment Update
Format: Online

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Description

Hiemstra Product Development, San Francisco, Calif., a leading product design and development company, has received Food and Drug Branch (FDB) approval from the California Department of Health Services' Division of Food, Drug and Radiation Safety to manufacture class I - III medical devices in its 750 sq. ft., class 10,000 CER (clean room). Hiemstra...

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