FDA Inspection 816456 — Aurident Inc
The FDA completed an inspection of Aurident Inc on Jan 29, 2013 in Fullerton, CA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.
Inspection Details
- Classification
- No Action Indicated (NAI)
- End Date
- Jan 29, 2013
- Fiscal Year
- 2013
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Fullerton, CA (United States)