FDA Inspection 682767 — Biomat USA Inc

Biomat USA Inc — FEI 2077838

The FDA completed an inspection of Biomat USA Inc on Sep 29, 2010 in Phoenix, 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
Sep 29, 2010
Fiscal Year
2010
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Phoenix, AZ (United States)