FDA inspection

Ionisos: FDA inspection ending May 19, 2004

FDA inspection 329333 · No Action Indicated (NAI) · Dagneux

Key facts

Inspection ID 329333
Firm Ionisos
FEI number 3003110073
Address Parc Dombes Cotiere Activites
City Dagneux
Fiscal year 2004
Inspection end date May 19, 2004
Classification No Action Indicated (NAI)
Project area Product Evaluation: Med Devices
Product type Devices

At a glance

  • None Citations
  • None 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