FDA Inspection
FUJIFILM Diosynth Biotechnologies Denmark ApSFUJIFILM Diosynth Biotechnologies Denmark ApS – FDA Inspection, Oct 31, 2017
Record Details
This FDA Inspection record concerns FUJIFILM Diosynth Biotechnologies Denmark ApS, with an inspection on October 31, 2017, issued by the Office of Inspections and Investigations, covering human drugs.
- Inspection Date
- October 31, 2017
- Product Type
- Human Drugs
- Person
- Michael Shanks (Issuing Officer)
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ID · 2918676d-486e-4fa0-9a60-9151bf9f52b4
Inspection Facts
- Inspection number
- 1030927
- 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 | |
| April 13, 2018 | 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 1052912 - 2018-04-13
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