FDA Inspection 1282052 — Matsuyama Seika Corp.

Matsuyama Seika Corp. — FEI 3004286637

The FDA completed an inspection of Matsuyama Seika Corp. on September 5, 2025 in Seki. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 4 citations were issued during this inspection. Product area: Food/Cosmetics.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
September 5, 2025
Fiscal Year
2025
Product Type
Food/Cosmetics
Project Area
Foodborne Biological Hazards
Location
Seki (Japan)

Citations

IDCFRDescription
2271421 CFR 117.410(c)Supply-chain program - Assurance (Adequate)
2271721 CFR 117.130(a)(1)Hazard analysis - Identification of hazard
2271921 CFR 117.135(c)(2)Allergen preventive controls - Appropriate (Adequate)
2272021 CFR 117.135(c)(3)Sanitation preventive controls - Appropriate (Adequate)