FDA Inspection 968511 — Mizuho OSI
The FDA completed an inspection of Mizuho OSI on Feb 25, 2016 in Union City, CA. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.
Inspection details
- Classification
- No Action Indicated (NAI)
- End Date
- Feb 25, 2016
- Fiscal Year
- 2016
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Union City, CA (United States)