FDA Inspection 1053346 — Biomat USA, Inc.

Biomat USA, Inc. — FEI 3011853315

The FDA completed an inspection of Biomat USA, Inc. on Apr 6, 2018 in Cedar 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
Apr 6, 2018
Fiscal Year
2018
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Cedar City, UT (United States)