FDA Inspection 932372 — Biomat USA Inc

Biomat USA Inc — FEI 3000717632

The FDA completed an inspection of Biomat USA Inc on Jun 30, 2015 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
Jun 30, 2015
Fiscal Year
2015
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Toledo, OH (United States)