FDA inspection

Ajinomoto Co., Inc.: FDA inspection ending Sep 27, 2013

FDA inspection 859572 · Voluntary Action Indicated (VAI) · Saga

Key facts

Inspection ID 859572
Firm Ajinomoto Co., Inc.
FEI number 3002806335
Address Ajinomoto (Kabu) Kyushukojo, Morodomicho 450; Morodomichooazamorodomitsu; Morodomichooazamorodomitsu; Morodomichooazamorodomitsu
City Saga
Country Japan
Fiscal year 2013
Inspection end date Sep 27, 2013
Classification Voluntary Action Indicated (VAI)
Project area Drug Quality Assurance
Product type Drugs

At a glance

  • None Citations
  • 1–9 Posted citations
  • No Warning letter followed
  • Yes Form FDA 483 issued
  • No Establishment inspection report (EIR) exists
  • 1–9 Inspections at this FEI

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About FDA inspections

FDA inspections are classified as No Action Indicated (NAI), Voluntary Action Indicated (VAI) or Official Action Indicated (OAI). Inspections of individual clinical investigators are not published here.

Source: U.S. Food and Drug Administration (FDA), inspection classification data

Browse all FDA inspections