FDA Inspection 975837 — Biomat USA, Inc

Biomat USA, Inc — FEI 1770171

The FDA completed an inspection of Biomat USA, Inc on Jun 1, 2016 in Salt Lake City, UT. 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 1, 2016
Fiscal Year
2016
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Salt Lake City, UT (United States)