FDA inspection

ARCHEON: FDA inspection ending Sep 19, 2025

FDA inspection 1286532 · Voluntary Action Indicated (VAI) · Besancon

Key facts

Inspection ID 1286532
Firm ARCHEON
FEI number 3017708978
Address 2 Chemin Des Aiguillettes
City Besancon
Country France
Fiscal year 2025
Inspection end date Sep 19, 2025
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

Browse all FDA inspections