FDA Inspection 1122741 — Biomat USA, Inc.

Biomat USA, Inc. — FEI 3007094934

The FDA completed an inspection of Biomat USA, Inc. on March 13, 2020 in Saint Paul, MN. 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 13, 2020
Fiscal Year
2020
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Saint Paul, MN (United States)