FDA Inspection 1309990 - FujiFilm Diosynth Biotechnologies U.S.A., Inc. - March 27, 2026

FDA Inspection 1309990 for FujiFilm Diosynth Biotechnologies U.S.A., Inc. on March 27, 2026. Classification: N/A.

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Record Summary

FDA Inspection 1309990 for FujiFilm Diosynth Biotechnologies U.S.A., Inc. on March 27, 2026. Classification: N/A.

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Record Information

Company

FujiFilm Diosynth Biotechnologies U.S.A., Inc.

Inspection Date

March 27, 2026

Product Type

Human Drugs

Office

Atlanta District Office

ID: 6a45f213-b711-4a42-b1b1-724099c2a16d

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