FDA Inspection 1196124 — Biomat USA Inc

Biomat USA Inc — FEI 3005601885

The FDA completed an inspection of Biomat USA Inc on Jan 13, 2023 in Des Moines, IA. 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 13, 2023
Fiscal Year
2023
Product Type
Biologics
Project Area
Vaccines and Allergenic Products
Location
Des Moines, IA (United States)