FDA Inspection 838107 — Biomat USA Inc

Biomat USA Inc — FEI 3007166152

The FDA completed an inspection of Biomat USA Inc on Jul 2, 2013 in Dayton, 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
Jul 2, 2013
Fiscal Year
2013
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Dayton, OH (United States)