FDA Inspection 1297602 — Biomat USA, Inc.

Biomat USA, Inc. — FEI 3013360213

The FDA completed an inspection of Biomat USA, Inc. on December 18, 2025 in Griffith, IN. 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
Griffith, IN (United States)