FDA Inspection 1059784 — Biomat USA, Inc

Biomat USA, Inc — FEI 3003908049

The FDA completed an inspection of Biomat USA, Inc on Jul 18, 2018 in Houston, TX. 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
Jul 18, 2018
Fiscal Year
2018
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Houston, TX (United States)