FDA inspection

Dyn'r: FDA inspection ending Sep 13, 2018

FDA inspection 1075894 · No Action Indicated (NAI) · Aix-En-Provence

Key facts

Inspection ID 1075894
Firm Dyn'r
FEI number 3008317830
Address 35 Rue Pierre Simon Laplace, Les Milles
City Aix-En-Provence
Country France
Fiscal year 2018
Inspection end date Sep 13, 2018
Classification No Action Indicated (NAI)
Project area Compliance: Devices
Product type Devices

At a glance

  • None 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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