FDA Inspection 701934 — Biomat USA, Inc.

Biomat USA, Inc. — FEI 3002793370

The FDA completed an inspection of Biomat USA, Inc. on November 19, 2010 in Wichita Falls, TX. 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 19, 2010
Fiscal Year
2011
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Wichita Falls, TX (United States)