FDA Inspection 870122 — FUJIFILM Healthcare Manufacturing Corp.
The FDA completed an inspection of FUJIFILM Healthcare Manufacturing Corp. on February 19, 2014 in Hanamaki. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.
Inspection Details
- Classification
- No Action Indicated (NAI) (NAI)
- End Date
- February 19, 2014
- Fiscal Year
- 2014
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Hanamaki (Japan)