FDA Inspection 1112924 — Biomat USA Inc

Biomat USA Inc — FEI 1718620

The FDA completed an inspection of Biomat USA Inc on November 7, 2019 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
November 7, 2019
Fiscal Year
2020
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Aurora, CO (United States)