FDA Inspection 808134 — Biomat USA, Inc

Biomat USA, Inc — FEI 2072896

The FDA completed an inspection of Biomat USA, Inc on November 8, 2012 in Laredo, 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 8, 2012
Fiscal Year
2013
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Laredo, TX (United States)