FDA Inspection 760924 — Biomat USA, Inc

Biomat USA, Inc — FEI 1037531

The FDA completed an inspection of Biomat USA, Inc on December 22, 2011 in Tuscaloosa, AL. 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 22, 2011
Fiscal Year
2012
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Tuscaloosa, AL (United States)