FDA Inspection 1030379 — FUJIFILM Diosynth Biotechnologies Denmark ApS
The FDA completed an inspection of FUJIFILM Diosynth Biotechnologies Denmark ApS on Jun 16, 2017 in Hillerod. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Drugs.
Inspection details
- Classification
- No Action Indicated (NAI)
- End Date
- Jun 16, 2017
- Fiscal Year
- 2017
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Hillerod (Denmark)