FDA Inspection 1057656 — Ajinomoto Omnichem NV

Ajinomoto Omnichem NV — FEI 3002807802

The FDA completed an inspection of Ajinomoto Omnichem NV on June 22, 2018 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: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
June 22, 2018
Fiscal Year
2018
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Wetteren (Belgium)