FDA Inspection 969080 — Biomat USA Inc

Biomat USA Inc — FEI 3005601885

The FDA completed an inspection of Biomat USA Inc on Apr 27, 2016 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
Apr 27, 2016
Fiscal Year
2016
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Des Moines, IA (United States)