FDA Inspection 839544 — Biomat USA, Inc.

Biomat USA, Inc. — FEI 3005480268

The FDA completed an inspection of Biomat USA, Inc. on July 3, 2013 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
July 3, 2013
Fiscal Year
2013
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Killeen, TX (United States)