FDA Inspection 755921 — Ajinomoto Omnichem

Ajinomoto Omnichem — FEI 3003677791

The FDA completed an inspection of Ajinomoto Omnichem on November 10, 2011 in Balen. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
November 10, 2011
Fiscal Year
2012
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Balen (Belgium)