FDA Inspection 1276853 — Biomat USA, Inc.
The FDA completed an inspection of Biomat USA, Inc. on Jul 16, 2025 in Midwest City, OK. 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
- Jul 16, 2025
- Fiscal Year
- 2025
- Product Type
- Biologics
- Project Area
- Blood and Blood Products
- Location
- Midwest City, OK (United States)