FDA Inspection 1331950 — Ajinomoto Omnichem NV

Ajinomoto Omnichem NV — FEI 3002807802

The FDA completed an inspection of Ajinomoto Omnichem NV on Jun 13, 2025 in Wetteren. 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: Veterinary.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Jun 13, 2025
Fiscal Year
2025
Product Type
Veterinary
Project Area
Monitoring of Marketed Animal Drugs, Feed, and Devices
Location
Wetteren (Belgium)

Additional Details

Mutual Recognition Agreement (MRA)

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