FDA Inspection 1254722 — Biomat USA Inc.

Biomat USA Inc. — FEI 3007960092

The FDA completed an inspection of Biomat USA Inc. on November 14, 2024 in Elgin, 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 14, 2024
Fiscal Year
2025
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Elgin, IL (United States)