FDA Inspection 1259453 — Biomat USA, Inc.

Biomat USA, Inc. — FEI 3005600120

The FDA completed an inspection of Biomat USA, Inc. on December 19, 2024 in Portland, OR. 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 19, 2024
Fiscal Year
2025
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Portland, OR (United States)