FDA Inspection
FUJIFILM Diosynth Biotechnologies Denmark ApSFUJIFILM Diosynth Biotechnologies Denmark ApS – FDA Inspection, Feb 12, 2019
Record Details
This FDA Inspection record concerns FUJIFILM Diosynth Biotechnologies Denmark ApS, with an inspection on February 12, 2019, issued by the Office of Inspections and Investigations, covering human drugs.
- Inspection Date
- February 12, 2019
- Product Type
- Human Drugs
View Company Profile
ID · 3b6bda6e-28b6-4236-a023-7a0258ac1a76
Inspection Facts
- Inspection number
- 1084340
- 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 |
| 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 1257821 - 2024-11-12
- FDA Inspection 1230111 - 2023-06-30
- FDA Inspection 1123030 - 2019-05-10
- FDA Inspection 1052912 - 2018-04-13
- FDA Inspection 1030927 - 2017-10-31
Document or profile
One record shows the event. A profile shows the pattern.
Buy this document for the source file and details behind this single event.
Choose full profile access to connect related records, sites, people, citations, and enforcement history in one view.