FDA Inspection 1026015 — Biomat USA, Inc

Biomat USA, Inc — FEI 3003826898

The FDA completed an inspection of Biomat USA, Inc on June 21, 2017 in Fort Worth, TX. 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
June 21, 2017
Fiscal Year
2017
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Fort Worth, TX (United States)