FDA Inspection 822777 — Biomat USA, Inc.

Biomat USA, Inc. — FEI 3003537708

The FDA completed an inspection of Biomat USA, Inc. on March 7, 2013 in Boca Raton, FL. 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 7, 2013
Fiscal Year
2013
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Boca Raton, FL (United States)