FDA inspection

Ionisos: FDA inspection ending Apr 5, 2024

FDA inspection 1237221 · Voluntary Action Indicated (VAI) · Sable Sur Sarthe

Key facts

Inspection ID 1237221
Firm Ionisos
FEI number 3002807295
Address Z.A. De L'Aubree
City Sable Sur Sarthe
Country France
Fiscal year 2024
Inspection end date Apr 5, 2024
Classification Voluntary Action Indicated (VAI)
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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