FDA Inspection 1281850 — Shinoda LLC

Shinoda LLC — FEI 3004506571

The FDA completed an inspection of Shinoda LLC on July 29, 2025 in Oceanside, CA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Food/Cosmetics.

Inspection Details

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