FDA Inspection 590718 — N.V. Organon
The FDA completed an inspection of N.V. Organon on May 14, 2009 in Oss. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Drugs.
Inspection details
- Classification
- No Action Indicated (NAI)
- End Date
- May 14, 2009
- Fiscal Year
- 2009
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Oss (Netherlands)