FDA Inspection 1291256 — Ajinomoto Co., Inc.

Ajinomoto Co., Inc. — FEI 3002806334

The FDA completed an inspection of Ajinomoto Co., Inc. on November 14, 2025 in Yokkaichi. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
November 14, 2025
Fiscal Year
2026
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Yokkaichi (Japan)