FDA Inspection 652380 — Amrex Zetron Inc
The FDA completed an inspection of Amrex Zetron Inc on March 16, 2010 in Paramount, 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 16, 2010
- Fiscal Year
- 2010
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Paramount, CA (United States)