FDA Inspection 1230771 — Biomat USA Inc

Biomat USA Inc — FEI 3020711716

The FDA completed an inspection of Biomat USA Inc on Jan 31, 2024 in Wood River, IL. 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
Jan 31, 2024
Fiscal Year
2024
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Wood River, IL (United States)