FDA Inspection 739997 — Biomat USA Inc

Biomat USA Inc — FEI 3000717632

The FDA completed an inspection of Biomat USA Inc on Aug 17, 2011 in Toledo, OH. 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
Aug 17, 2011
Fiscal Year
2011
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Toledo, OH (United States)