FDA Inspection 1342196 — Wyeth Lederle S.R.L
The FDA completed an inspection of Wyeth Lederle S.R.L on Nov 15, 2024 in Catania. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Drugs.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI)
- End Date
- Nov 15, 2024
- Fiscal Year
- 2025
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Catania (Italy)
Additional Details
Mutual Recognition Agreement (MRA)