FDA Inspection 1042704 — Biomat USA, Inc

Biomat USA, Inc — FEI 1640366

The FDA completed an inspection of Biomat USA, Inc on December 15, 2017 in Denver, CO. 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
December 15, 2017
Fiscal Year
2018
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Denver, CO (United States)