FDA Inspection 903957 — Biomat USA, Inc.

Biomat USA, Inc. — FEI 1971882

The FDA completed an inspection of Biomat USA, Inc. on November 14, 2014 in Saint Louis, MO. 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 14, 2014
Fiscal Year
2015
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Saint Louis, MO (United States)