# FDA Inspection 1286532 - ARCHEON - September 19, 2025

Source: https://www.keypedia.com/records/fda_inspections/archeon/345a5833-2b64-4fe6-a755-b0e393cf349f
Source feed: FDA_Inspections

> FDA Inspection 1286532 for ARCHEON on September 19, 2025. Classification: Voluntary Action Indicated (VAI).

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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)
- Project Area: Postmarket Assurance: Medical Devices
- Product Type: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1286532 - 2025-09-19](https://www.keypedia.com/records/fda_inspections/archeon/1a209d6b-77be-4574-8031-98491d4367b9)
- [FDA Inspection 1286532 - 2025-09-19](https://www.keypedia.com/records/fda_inspections/archeon/91e6a6ad-a604-45a5-86d1-b739c13c2205)
- [FDA Inspection 1286532 - 2025-09-19](https://www.keypedia.com/records/fda_inspections/archeon/c36199e8-4c7d-4181-83af-c7e5bd4afb51)

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

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7