FDA Inspection 859572 — Ajinomoto Co., Inc.

Ajinomoto Co., Inc. — FEI 3002806335

The FDA completed an inspection of Ajinomoto Co., Inc. on Sep 27, 2013 in Saga. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Sep 27, 2013
Fiscal Year
2013
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Saga (Japan)

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