FDA Inspection 1261618 — Ajinomoto Company Inc.

Ajinomoto Company Inc. — FEI 3002806336

The FDA completed an inspection of Ajinomoto Company Inc. on February 21, 2025 in Kawasaki-City. 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
February 21, 2025
Fiscal Year
2025
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Kawasaki-City (Japan)