FDA Inspection 1254221 — Biomat USA, Inc.

Biomat USA, Inc. — FEI 1000135246

The FDA completed an inspection of Biomat USA, Inc. on Nov 6, 2024 in Bakersfield, CA. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Nov 6, 2024
Fiscal Year
2025
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Bakersfield, CA (United States)