FDA Inspection 1178127 — Wyeth Lederle S.R.L
The FDA completed an inspection of Wyeth Lederle S.R.L on Jan 21, 2022 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
- Jan 21, 2022
- Fiscal Year
- 2022
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Catania (Italy)
Additional details
Mutual Recognition Agreement (MRA)