FDA Inspection 1289250 — Biomat USA Inc

Biomat USA Inc — FEI 3022477122

The FDA completed an inspection of Biomat USA Inc on November 6, 2025 in Killeen, TX. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 1 citation was issued during this inspection. Product area: Biologics.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
November 6, 2025
Fiscal Year
2026
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Killeen, TX (United States)

Citations

IDCFRDescription
9821 CFR 606.100(c)Thorough investigations