FDA Inspection 822925 — Arbor Vita Corporation
The FDA completed an inspection of Arbor Vita Corporation on March 18, 2013 in Fremont, CA. 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 18, 2013
- Fiscal Year
- 2013
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Fremont, CA (United States)