FDA Inspection
FUJIFILM Diosynth Biotechnologies Denmark ApSFUJIFILM Diosynth Biotechnologies Denmark ApS – FDA Inspection, Nov 12, 2024
Record Details
This FDA Inspection record concerns FUJIFILM Diosynth Biotechnologies Denmark ApS, with an inspection on November 12, 2024, issued by the Office of Inspections and Investigations, covering human drugs.
- Inspection Date
- November 12, 2024
- Product Type
- Human Drugs
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ID · 2e61f960-1dde-4dbe-83d0-3ed888339059
Inspection Facts
- Inspection number
- 1257821
- FDA center
- Human Drugs
Other FDA inspections of FUJIFILM Diosynth Biotechnologies Denmark ApS
9| Date | Classification | Office | Project area |
|---|---|---|---|
| June 30, 2023 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| May 10, 2019 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| February 12, 2019 | Not classified | Office of Inspections and Investigations | |
| April 13, 2018 | Not classified | Office of Inspections and Investigations | |
| October 31, 2017 | Not classified | Office of Inspections and Investigations |
Other documents for FUJIFILM Diosynth Biotechnologies Denmark ApS
- FDA Inspection 1230111 - 2023-06-30
- FDA Inspection 1123030 - 2019-05-10
- FDA Inspection 1084340 - 2019-02-12
- FDA Inspection 1052912 - 2018-04-13
- FDA Inspection 1030927 - 2017-10-31
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