FDA Inspection 800290 — Biomat USA Inc.
The FDA completed an inspection of Biomat USA Inc. on Sep 20, 2012 in Saint Paul, MN. 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
- Sep 20, 2012
- Fiscal Year
- 2012
- Product Type
- Biologics
- Project Area
- Blood and Blood Products
- Location
- Saint Paul, MN (United States)