FDA Inspection 679053 - FujiFilm Diosynth Biotechnologies U.S.A., Inc. - July 16, 2010
FDA Inspection 679053 for FujiFilm Diosynth Biotechnologies U.S.A., Inc. on July 16, 2010. Classification: No Action Indicated (NAI).
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FDA Inspection 679053 for FujiFilm Diosynth Biotechnologies U.S.A., Inc. on July 16, 2010. Classification: No Action Indicated (NAI).
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Inspection Date
July 16, 2010
Product Type
Drugs
ID: ce785a7c-4ddc-4846-999a-3efbae967b1d
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