FDA Inspection 1298210 — Biomat USA, Inc

Biomat USA, Inc — FEI 3003885812

The FDA completed an inspection of Biomat USA, Inc on December 18, 2025 in Frederick, MD. 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
December 18, 2025
Fiscal Year
2026
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Frederick, MD (United States)