FDA Inspection 755921 — Ajinomoto Omnichem

Ajinomoto Omnichem — FEI 3003677791

The FDA completed an inspection of Ajinomoto Omnichem on Nov 10, 2011 in Balen. 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
Nov 10, 2011
Fiscal Year
2012
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Balen (Belgium)

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