FDA Inspection 1292718 — Biomat USA Inc.

Biomat USA Inc. — FEI 3023833901

The FDA completed an inspection of Biomat USA Inc. on November 19, 2025 in Chicago, IL. 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
November 19, 2025
Fiscal Year
2026
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Chicago, IL (United States)