FDA Inspection 637083 — Wyeth Lederle S.R.L
The FDA completed an inspection of Wyeth Lederle S.R.L on Dec 4, 2009 in Catania. 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
- Dec 4, 2009
- Fiscal Year
- 2010
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Catania (Italy)