FDA Inspection 685689 — N.V. Organon

N.V. Organon — FEI 3002806821

The FDA completed an inspection of N.V. Organon on July 2, 2010 in Oss. 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
July 2, 2010
Fiscal Year
2010
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Oss (Netherlands)