FDA Inspection 869722 — Biomat USA Inc

Biomat USA Inc — FEI 1718620

The FDA completed an inspection of Biomat USA Inc on March 4, 2014 in Aurora, CO. 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
March 4, 2014
Fiscal Year
2014
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Aurora, CO (United States)