FDA Inspection
FUJIFILM Diosynth Biotechnologies Denmark ApSFUJIFILM Diosynth Biotechnologies Denmark ApS – FDA Inspection, Apr 13, 2018
Record Details
This FDA Inspection record concerns FUJIFILM Diosynth Biotechnologies Denmark ApS, with an inspection on April 13, 2018, issued by the Office of Inspections and Investigations, covering human drugs.
- Inspection Date
- April 13, 2018
- Product Type
- Human Drugs
- Person
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ID · 5d0b36e8-6a9e-40ed-a1f0-176156dc7bc2
Inspection Facts
- Inspection number
- 1052912
- FDA center
- Human Drugs
- Outcome
- Form 483 issued
Other FDA inspections of FUJIFILM Diosynth Biotechnologies Denmark ApS
9| Date | Classification | Office | Project area |
|---|---|---|---|
| November 12, 2024 | Not classified | Office of Inspections and Investigations | |
| 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 | |
| October 31, 2017 | Not classified | Office of Inspections and Investigations |
Other documents for FUJIFILM Diosynth Biotechnologies Denmark ApS
- FDA Inspection 1257821 - 2024-11-12
- FDA Inspection 1230111 - 2023-06-30
- FDA Inspection 1123030 - 2019-05-10
- FDA Inspection 1084340 - 2019-02-12
- FDA Inspection 1030927 - 2017-10-31
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