FDA inspection

Echosens: FDA inspection ending Feb 1, 2017

FDA inspection 1003219 · Voluntary Action Indicated (VAI) · Paris

Key facts

Inspection ID 1003219
Firm Echosens
FEI number 3010258456
Address 30 Place D Italie
City Paris
Country France
Fiscal year 2017
Inspection end date Feb 1, 2017
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
  • 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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