FDA Inspection 792624 — Wyeth Lederle S.R.L

Wyeth Lederle S.R.L — FEI 3002806766

The FDA completed an inspection of Wyeth Lederle S.R.L on Jul 20, 2012 in Catania. The inspection was classified OAI (Official Action Indicated — regulatory and/or administrative actions are recommended). Product area: Drugs.

Inspection details

Classification
Official Action Indicated (OAI)
End Date
Jul 20, 2012
Fiscal Year
2012
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Catania (Italy)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.