FDA inspection

Sanofi S.r.l.: FDA inspection ending Jun 23, 2011

FDA inspection 734695 · Voluntary Action Indicated (VAI) · Anagni

Key facts

Inspection ID 734695
Firm Sanofi S.r.l.
FEI number 3002807108
Address Via Valcanello 4
City Anagni
Country Italy
Fiscal year 2011
Inspection end date Jun 23, 2011
Classification Voluntary Action Indicated (VAI)
Project area Postmarket Assurance: Devices
Product type Devices

At a glance

  • 1–9 Citations
  • 1–9 Posted citations
  • No Warning letter followed
  • Yes Form FDA 483 issued
  • Yes Establishment inspection report (EIR) exists
  • 10–99 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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