FDA Inspection 1037713 — FUJIFILM Corporation Medical Systems Research & Development Center Kashiwa
The FDA completed an inspection of FUJIFILM Corporation Medical Systems Research & Development Center Kashiwa on Dec 21, 2017 in Kashiwa. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Devices.
Inspection details
- Classification
- Voluntary Action Indicated (VAI)
- End Date
- Dec 21, 2017
- Fiscal Year
- 2018
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Kashiwa (Japan)