FDA Inspection 792624 — Wyeth Lederle S.r.l
The FDA completed an inspection of Wyeth Lederle S.r.l on July 20, 2012 in Catania. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). Product area: Drugs.
Inspection Details
- Classification
- Official Action Indicated (OAI) (OAI)
- End Date
- July 20, 2012
- Fiscal Year
- 2012
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Catania (Italy)