FDA inspection

Wyeth Lederle S.r.l: FDA inspection ending Apr 20, 2017

FDA inspection 1012188 · Voluntary Action Indicated (VAI) · Catania

Key facts

Inspection ID 1012188
Firm Wyeth Lederle S.r.l
FEI number 3002806766
Address Zona Industriale, Via Franco Gorgone 6A
City Catania
Country Italy
Fiscal year 2017
Inspection end date Apr 20, 2017
Classification Voluntary Action Indicated (VAI)
Project area Drug Quality Assurance
Product type Drugs

At a glance

  • 1–9 Citations
  • 1–9 Posted citations
  • No Warning letter followed
  • Yes Form FDA 483 issued
  • No Establishment inspection report (EIR) exists
  • 1–9 Inspections at this FEI

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About FDA inspections

FDA inspections are classified as No Action Indicated (NAI), Voluntary Action Indicated (VAI) or Official Action Indicated (OAI). Inspections of individual clinical investigators are not published here.

Source: U.S. Food and Drug Administration (FDA), inspection classification data

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