FDA inspection

RICARIMPEX SAS CO.: FDA inspection ending Sep 20, 2017

FDA inspection 1026687 · Voluntary Action Indicated (VAI) · Eysines

Key facts

Inspection ID 1026687
Firm RICARIMPEX SAS CO.
FEI number 3009106257
Address 245 Avenue De Saint Medard
City Eysines
Country France
Fiscal year 2017
Inspection end date Sep 20, 2017
Classification Voluntary Action Indicated (VAI)
Project area Compliance: 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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