FDA Inspection 1114409 — FUJIFILM Healthcare Manufacturing Corporation Sano Office
The FDA completed an inspection of FUJIFILM Healthcare Manufacturing Corporation Sano Office on Sep 10, 2019 in Sano. The inspection was classified OAI (Official Action Indicated — regulatory and/or administrative actions are recommended). Product area: Devices.
Inspection Details
- Classification
- Official Action Indicated (OAI)
- End Date
- Sep 10, 2019
- Fiscal Year
- 2019
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Sano (Japan)