FDA Inspection 1000746 — Biomat USA, Inc

Biomat USA, Inc — FEI 1876548

The FDA completed an inspection of Biomat USA, Inc on Jan 13, 2017 in Colorado Springs, CO. 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
Jan 13, 2017
Fiscal Year
2017
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Colorado Springs, CO (United States)