FDA Inspection 709479 — Biomat USA, Inc

Biomat USA, Inc — FEI 2084085

The FDA completed an inspection of Biomat USA, Inc on Feb 14, 2011 in Mesa, AZ. 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
Feb 14, 2011
Fiscal Year
2011
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Mesa, AZ (United States)