FDA Inspection 862866 — Biomat USA, Inc.

Biomat USA, Inc. — FEI 3007094934

The FDA completed an inspection of Biomat USA, Inc. on January 17, 2014 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
January 17, 2014
Fiscal Year
2014
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Saint Paul, MN (United States)