FDA Inspection 814820 — Biomat USA Inc
The FDA completed an inspection of Biomat USA Inc on January 18, 2013 in Moorhead, MN. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Biologics.
Inspection Details
- Classification
- No Action Indicated (NAI) (NAI)
- End Date
- January 18, 2013
- Fiscal Year
- 2013
- Product Type
- Biologics
- Project Area
- Blood and Blood Products
- Location
- Moorhead, MN (United States)