FDA Inspection 960600 — Aomori Olympus Co., Ltd.
The FDA completed an inspection of Aomori Olympus Co., Ltd. on March 2, 2016 in Kuroishi. 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
- March 2, 2016
- Fiscal Year
- 2016
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Kuroishi (Japan)