FDA Inspection 1207801 — Ajinomoto Omnichem

Ajinomoto Omnichem — FEI 3003677791

The FDA completed an inspection of Ajinomoto Omnichem on December 16, 2022 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
December 16, 2022
Fiscal Year
2023
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Balen (Belgium)

Additional Details

Mutual Recognition Agreement (MRA)