FDA Inspection 1150333 - FUJIFILM Diosynth Biotechnologies Texas, LLC - August 31, 2021

FDA Inspection 1150333 for FUJIFILM Diosynth Biotechnologies Texas, LLC on August 31, 2021. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 1150333 for FUJIFILM Diosynth Biotechnologies Texas, LLC on August 31, 2021. Classification: Voluntary Action Indicated (VAI).

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Record Information

Company

FUJIFILM Diosynth Biotechnologies Texas, LLC

Inspection Date

August 31, 2021

Product Type

Biologics

Office

Center for Biologics Evaluation and Research

ID: 85c18c69-e866-4ac8-81de-0c96e655d2d1

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