FDA Inspection
FUJIFILM Diosynth Biotechnologies UK LimitedFUJIFILM Diosynth Biotechnologies UK Limited – FDA Inspection, Sep 1, 2026
Record Details
This FDA Inspection record concerns FUJIFILM Diosynth Biotechnologies UK Limited, with an inspection on September 1, 2026, issued by the Office of Inspections and Investigations, covering human drugs.
- Inspection Date
- September 1, 2026
- Product Type
- Human Drugs
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ID · 0a62dc79-bae4-40e3-85e2-01849cc7cb02
Inspection Facts
- Inspection number
- 1339338
- FDA center
- Human Drugs
Other FDA inspections of FUJIFILM Diosynth Biotechnologies UK Limited
6| Date | Classification | Office | Project area |
|---|---|---|---|
| March 17, 2023 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| March 25, 2021 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| November 16, 2018 | Not classified | Office of Inspections and Investigations | |
| July 11, 2014 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| June 20, 2012 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for FUJIFILM Diosynth Biotechnologies UK Limited
- FDA Inspection 1200417 - 2023-03-17
- FDA Inspection 1155694 - 2021-03-25
- FDA Inspection 1097949 - 2018-11-16
- FDA Inspection 894612 - 2014-07-11
- FDA Inspection 790405 - 2012-06-20
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