FDA Inspection 1117568 — Biomat USA Inc

Biomat USA Inc — FEI 3005523333

The FDA completed an inspection of Biomat USA Inc on January 24, 2020 in Richmond, VA. 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
January 24, 2020
Fiscal Year
2020
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Richmond, VA (United States)