FDA Inspection 722053 — Biomat USA, Inc.

Biomat USA, Inc. — FEI 1971882

The FDA completed an inspection of Biomat USA, Inc. on April 27, 2011 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
April 27, 2011
Fiscal Year
2011
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Saint Louis, MO (United States)