FDA Inspection 1285048 — KANEMATSU USA INC.

KANEMATSU USA INC. — FEI 3022995303

The FDA completed an inspection of KANEMATSU USA INC. on September 29, 2025 in San Jose, CA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 2 citations were issued during this inspection. Product area: Food/Cosmetics.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
September 29, 2025
Fiscal Year
2025
Product Type
Food/Cosmetics
Project Area
Foodborne Biological Hazards
Location
San Jose, CA (United States)

Additional Details

FSVP

Citations

IDCFRDescription
1826321 CFR 1.504(b)(1)Hazard analysis biological, chemical, physical
1830321 CFR 1.506(e)(1)Verification activity before import, periodically