FDA inspection

Sanofi Winthrop Industrie: FDA inspection ending Dec 12, 2014

FDA inspection 909720 · Voluntary Action Indicated (VAI) · Sisteron

Key facts

Inspection ID 909720
Firm Sanofi Winthrop Industrie
FEI number 1000476619
Address 45 Chemin De Meteline, Boite Postale 15
City Sisteron
Country France
Fiscal year 2015
Inspection end date Dec 12, 2014
Classification Voluntary Action Indicated (VAI)
Project area Drug Quality Assurance
Product type Drugs

At a glance

  • None 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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