FDA Inspection 658222 — Biomat USA, Inc.

Biomat USA, Inc. — FEI 2176255

The FDA completed an inspection of Biomat USA, Inc. on Apr 8, 2010 in Milwaukee, WI. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Apr 8, 2010
Fiscal Year
2010
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Milwaukee, WI (United States)