FDA Inspection 991433 — Biomat USA, Inc.

Biomat USA, Inc. — FEI 3006256036

The FDA completed an inspection of Biomat USA, Inc. on Nov 4, 2016 in Saint Joseph, MO. 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
Nov 4, 2016
Fiscal Year
2017
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Saint Joseph, MO (United States)