FDA Inspection 790405 - FUJIFILM Diosynth Biotechnologies UK Limited - June 20, 2012

FDA Inspection 790405 for FUJIFILM Diosynth Biotechnologies UK Limited on June 20, 2012. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 790405 for FUJIFILM Diosynth Biotechnologies UK Limited on June 20, 2012. Classification: Voluntary Action Indicated (VAI).

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Record Information

Company

FUJIFILM Diosynth Biotechnologies UK Limited

Inspection Date

June 20, 2012

Product Type

Drugs

Office

Center for Drug Evaluation and Research

ID: 1bcd5941-78e2-460b-84e1-f5bf9c0b79be

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