FDA Inspection 809231 — Biomat USA Inc

Biomat USA Inc — FEI 3003824349

The FDA completed an inspection of Biomat USA Inc on Dec 5, 2012 in Texarkana, TX. 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
Dec 5, 2012
Fiscal Year
2013
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Texarkana, TX (United States)