FDA Inspection 637173 — Ajinomoto Omnichem NV
The FDA completed an inspection of Ajinomoto Omnichem NV on December 4, 2009 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
- December 4, 2009
- Fiscal Year
- 2010
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Wetteren (Belgium)