FDA inspection

Impeto Medical: FDA inspection ending Sep 16, 2015

FDA inspection 944840 · Voluntary Action Indicated (VAI) · Paris

Key facts

Inspection ID 944840
Firm Impeto Medical
FEI number 3008496197
Address 17 rue Campagne Premiere
City Paris
Country France
Fiscal year 2015
Inspection end date Sep 16, 2015
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

Browse all FDA inspections