# FDA Inspection 1280202 - Careox, Llc - August 29, 2025

Source: https://www.keypedia.com/records/fda_inspections/careox-llc/db4ee33d-c2bd-41cc-a04d-287a91039215
Source feed: FDA_Inspections

> FDA Inspection 1280202 for Careox, Llc on August 29, 2025. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1280202
- Company Name: Careox, Llc
- Inspection Date: 2025-08-29
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Medical Devices
- Product Type: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1280202 - 2025-08-29](https://www.keypedia.com/records/fda_inspections/careox-llc/8466b605-b552-4756-9804-4c8b08f384d8)
- [FDA Inspection 1280202 - 2025-08-29](https://www.keypedia.com/records/fda_inspections/careox-llc/d4c7369d-ad0c-46c4-b987-0aed253ec7dd)
- [FDA Inspection 1280202 - 2025-08-29](https://www.keypedia.com/records/fda_inspections/careox-llc/a8f7fe07-2bab-4637-9d54-c42f25ca6cc2)

Company: https://www.keypedia.com/companies/careox-llc/d12461e8-889a-4a6f-87ee-d0f3b88a30f1

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