FDA Inspection 894800 — VITA North America
The FDA completed an inspection of VITA North America on Sep 2, 2014 in Yorba Linda, 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
- Sep 2, 2014
- Fiscal Year
- 2014
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Yorba Linda, CA (United States)