FDA Inspection 1056221 — Biomat USA, Inc

Biomat USA, Inc — FEI 3003885812

The FDA completed an inspection of Biomat USA, Inc on April 20, 2018 in Frederick, MD. 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
April 20, 2018
Fiscal Year
2018
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Frederick, MD (United States)