FDA Inspection 867478 — Biomat USA Inc
The FDA completed an inspection of Biomat USA Inc on Feb 24, 2014 in Des Moines, IA. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Biologics.
Inspection Details
- Classification
- No Action Indicated (NAI)
- End Date
- Feb 24, 2014
- Fiscal Year
- 2014
- Product Type
- Biologics
- Project Area
- Blood and Blood Products
- Location
- Des Moines, IA (United States)