FDA Inspection 790446 — FUJIFILM Corporation Medical Systems Research & Development Center Kashiwa
The FDA completed an inspection of FUJIFILM Corporation Medical Systems Research & Development Center Kashiwa on Jun 7, 2012 in Kashiwa. 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
- Jun 7, 2012
- Fiscal Year
- 2012
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Kashiwa (Japan)