FDA Inspection 1200950 — FUJIFILM Healthcare Manufacturing Corp.
The FDA completed an inspection of FUJIFILM Healthcare Manufacturing Corp. on March 10, 2023 in Hanamaki. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Devices.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI) (VAI)
- End Date
- March 10, 2023
- Fiscal Year
- 2023
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Hanamaki (Japan)