FDA inspection

Anteis Sa: FDA inspection ending Nov 4, 2009

FDA inspection 630082 · Voluntary Action Indicated (VAI) · Plan-Les-Ouates

Key facts

Inspection ID 630082
Firm Anteis Sa
FEI number 3007744205
Address Chemin Des Aulx
City Plan-Les-Ouates
Country Switzerland
Fiscal year 2010
Inspection end date Nov 4, 2009
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
  • 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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