FDA Inspection 559762 - FUJIFILM Diosynth Biotechnologies UK Limited - January 09, 2009

FDA Inspection 559762 for FUJIFILM Diosynth Biotechnologies UK Limited on January 09, 2009. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 559762 for FUJIFILM Diosynth Biotechnologies UK Limited on January 09, 2009. Classification: Voluntary Action Indicated (VAI).

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Record Information

Company

FUJIFILM Diosynth Biotechnologies UK Limited

Inspection Date

January 9, 2009

Product Type

Drugs

Office

Center for Drug Evaluation and Research

ID: c84cbca7-11ac-472d-bf27-2b5b74009d5f

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