FDA Inspection 1200417 - FUJIFILM Diosynth Biotechnologies UK Limited - March 17, 2023

FDA Inspection 1200417 for FUJIFILM Diosynth Biotechnologies UK Limited on March 17, 2023. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 1200417 for FUJIFILM Diosynth Biotechnologies UK Limited on March 17, 2023. Classification: Voluntary Action Indicated (VAI).

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Record Information

Company

FUJIFILM Diosynth Biotechnologies UK Limited

Inspection Date

March 17, 2023

Product Type

Drugs

Office

Center for Drug Evaluation and Research

ID: 4d6a78ce-42f0-4143-ab86-759495398523

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