FDA Inspection 761546 — FUJIFILM Diosynth Biotechnologies Denmark ApS
The FDA completed an inspection of FUJIFILM Diosynth Biotechnologies Denmark ApS on Dec 2, 2011 in Hillerod. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.
Inspection details
- Classification
- No Action Indicated (NAI)
- End Date
- Dec 2, 2011
- Fiscal Year
- 2012
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Hillerod (Denmark)