FDA Inspection 1057668 — Ajinomoto Omnichem

Ajinomoto Omnichem — FEI 3003677791

The FDA completed an inspection of Ajinomoto Omnichem on June 29, 2018 in Balen. 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 29, 2018
Fiscal Year
2018
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Balen (Belgium)