FDA Inspection 894612 - FUJIFILM Diosynth Biotechnologies UK Limited - July 11, 2014

FDA Inspection 894612 for FUJIFILM Diosynth Biotechnologies UK Limited on July 11, 2014. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 894612 for FUJIFILM Diosynth Biotechnologies UK Limited on July 11, 2014. Classification: Voluntary Action Indicated (VAI).

Violation Codes

21 CFR 211.110(a)

21 CFR 211.160(b)

21 CFR 211.22(c)

21 CFR 211.25(a)

21 CFR 211.67(a)

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Record Information

Company

FUJIFILM Diosynth Biotechnologies UK Limited

Inspection Date

July 11, 2014

Product Type

Drugs

Office

Center for Drug Evaluation and Research

ID: ac5f17ff-d054-4ba5-9a1a-a21b8ebc2b8c

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