FDA Inspection 1115202 — FUJIFILM Healthcare Manufacturing Corporation Hitachiomiya Office
The FDA completed an inspection of FUJIFILM Healthcare Manufacturing Corporation Hitachiomiya Office on September 12, 2019 in Hitachiomiya. 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 12, 2019
- Fiscal Year
- 2019
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Hitachiomiya (Japan)