FDA Inspection 798908 — Ajinomoto Company Inc.

Ajinomoto Company Inc. — FEI 3002806336

The FDA completed an inspection of Ajinomoto Company Inc. on September 13, 2012 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
September 13, 2012
Fiscal Year
2012
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Kawasaki-City (Japan)