FDA Inspection 1038111 — Ajinomoto Company Inc.

Ajinomoto Company Inc. — FEI 3002806336

The FDA completed an inspection of Ajinomoto Company Inc. on September 22, 2017 in Kawasaki-City. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
September 22, 2017
Fiscal Year
2017
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Kawasaki-City (Japan)