FDA Inspection 859572 — Ajinomoto Co., Inc.

Ajinomoto Co., Inc. — FEI 3002806335

The FDA completed an inspection of Ajinomoto Co., Inc. on September 27, 2013 in Saga. 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 27, 2013
Fiscal Year
2013
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Saga (Japan)