FDA Inspection 985584 — Biomat USA Inc.
The FDA completed an inspection of Biomat USA Inc. on Sep 22, 2016 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 22, 2016
- Fiscal Year
- 2016
- Product Type
- Biologics
- Project Area
- Blood and Blood Products
- Location
- Saint Paul, MN (United States)