FDA Inspection 1038111 — Ajinomoto Company Inc.

Ajinomoto Company Inc. — FEI 3002806336

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

Inspection Details

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

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.