# FDA Inspection 1280564 - Clearadvance, LLC - September 04, 2025

Source: https://www.globalkeysolutions.net/records/fda_inspections/clearadvance-llc/aaf888e2-0e71-46de-9fcb-aedccbdef9f1
Source feed: FDA_Inspections

> FDA Inspection 1280564 for Clearadvance, LLC on September 04, 2025. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1280564
- Company Name: Clearadvance, LLC
- Inspection Date: 2025-09-04
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1280564 - 2025-09-04](https://www.globalkeysolutions.net/records/fda_inspections/clearadvance-llc/43655d11-2c1a-4817-a6c3-2129db8f9cf7)
- [FDA Inspection 1280564 - 2025-09-04](https://www.globalkeysolutions.net/records/fda_inspections/clearadvance-llc/effa19ac-78e0-4714-81c2-a72fdc13d309)
- [FDA Inspection 1280564 - 2025-09-04](https://www.globalkeysolutions.net/records/fda_inspections/clearadvance-llc/bcfa4316-1b82-4476-8f0e-9c1555282c5f)

Company: https://www.globalkeysolutions.net/companies/clearadvance-llc/769ed9c5-1e23-48cb-b055-7cd51384cdfa

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