FDA Inspection 1051875 — Biomat USA Inc.

Biomat USA Inc. — FEI 3007299028

The FDA completed an inspection of Biomat USA Inc. on April 27, 2018 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
April 27, 2018
Fiscal Year
2018
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Saint Paul, MN (United States)