FDA Inspection
FUJIFILM Diosynth Biotechnologies Denmark ApSFUJIFILM Diosynth Biotechnologies Denmark ApS – FDA Inspection, May 27, 2011
Record Details
This FDA Inspection record concerns FUJIFILM Diosynth Biotechnologies Denmark ApS, with an inspection on May 27, 2011, issued by the Center for Drug Evaluation and Research, covering drugs.
- Inspection Date
- May 27, 2011
- Product Type
- Drugs
View Company Profile
ID · 5d6fe364-ad2f-4c8f-b933-0d12bd322f17
Inspection Facts
No Action Indicated (NAI)
No objectionable conditions or practices were found during the inspection.
- Inspection number
- 737746
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
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
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.