# ARCHEON – FDA Inspection, Sep 19, 2025

Source: https://www.keypedia.com/records/fda_inspections/archeon/1a209d6b-77be-4574-8031-98491d4367b9
Source feed: FDA_Inspections

> FDA inspection 1286532 of ARCHEON, September 19, 2025. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR parts 806 and 820. Form 483 issued.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1286532
- Company Name: ARCHEON
- Inspection Date: 2025-09-19
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Medical Devices
- Product Type: Medical Devices & Rad Health
- Center: Medical Devices & Rad Health
- Office Name: Office of Inspections and Investigations
- Citation Count: 2

## Related Officers

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Company: https://www.keypedia.com/companies/archeon/65ce6f58-3f2c-4ef9-a379-75d38e90c6ae

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