FDA Inspection 703149 — Biomat USA, Inc.

Biomat USA, Inc. — FEI 3005480268

The FDA completed an inspection of Biomat USA, Inc. on December 16, 2010 in Killeen, 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
December 16, 2010
Fiscal Year
2011
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Killeen, TX (United States)