FDA Inspection 989406 - FujiFilm Diosynth Biotechnologies U.S.A., Inc. - March 31, 2016
FDA Inspection 989406 for FujiFilm Diosynth Biotechnologies U.S.A., Inc. on March 31, 2016. Classification: No Action Indicated (NAI).
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FDA Inspection 989406 for FujiFilm Diosynth Biotechnologies U.S.A., Inc. on March 31, 2016. Classification: No Action Indicated (NAI).
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Inspection Date
March 31, 2016
Product Type
Drugs
ID: 8572110c-bf60-48d4-b637-a431e1705259
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