FDA Inspection 1114409 — FUJIFILM Healthcare Manufacturing Corporation Sano Office
The FDA completed an inspection of FUJIFILM Healthcare Manufacturing Corporation Sano Office on September 10, 2019 in Sano. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). Product area: Devices.
Inspection Details
- Classification
- Official Action Indicated (OAI) (OAI)
- End Date
- September 10, 2019
- Fiscal Year
- 2019
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Sano (Japan)