FDA Inspection 1045267 - FujiFilm Diosynth Biotechnologies U.S.A., Inc. - February 09, 2018
FDA Inspection 1045267 for FujiFilm Diosynth Biotechnologies U.S.A., Inc. on February 09, 2018. Classification: No Action Indicated (NAI).
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FDA Inspection 1045267 for FujiFilm Diosynth Biotechnologies U.S.A., Inc. on February 09, 2018. Classification: No Action Indicated (NAI).
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Inspection Date
February 9, 2018
Product Type
Drugs
ID: 956739fc-b00a-4194-b345-00f56129ccf1
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