FDA Inspection 1018966 — Biomat USA, Inc

Biomat USA, Inc — FEI 3007198312

The FDA completed an inspection of Biomat USA, Inc on July 20, 2017 in Cincinnati, OH. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
July 20, 2017
Fiscal Year
2017
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Cincinnati, OH (United States)