FDA Inspection 987961 — Ajinomoto Omnichem NV

Ajinomoto Omnichem NV — FEI 3002807802

The FDA completed an inspection of Ajinomoto Omnichem NV on October 5, 2016 in Wetteren. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Veterinary.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
October 5, 2016
Fiscal Year
2017
Product Type
Veterinary
Project Area
Monitoring of Marketed Animal Drugs, Feed, and Devices
Location
Wetteren (Belgium)