# FDA Inspection 1288408 - KSL Biomedical, Inc. - October 24, 2025

Source: https://www.keypedia.com/records/fda_inspections/ksl-biomedical-inc/066cff9b-bab2-4e9b-9b5a-d5d9d39b00b7
Source feed: FDA_Inspections

> FDA Inspection 1288408 for KSL Biomedical, Inc. on October 24, 2025. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1288408
- Company Name: KSL Biomedical, Inc.
- Inspection Date: 2025-10-24
- 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 1288408 - 2025-10-24](https://www.keypedia.com/records/fda_inspections/ksl-biomedical-inc/9e8767df-22c8-4872-a9c6-e6fd3367c367)
- [FDA Inspection 1288408 - 2025-10-24](https://www.keypedia.com/records/fda_inspections/ksl-biomedical-inc/3d2f6667-f821-4733-835b-5087cbed2b52)
- [FDA Inspection 1288408 - 2025-10-24](https://www.keypedia.com/records/fda_inspections/ksl-biomedical-inc/5d9827d6-f1d4-4e72-9128-f2fd9f8b3330)

Company: https://www.keypedia.com/companies/ksl-biomedical-inc/061c6425-9031-4e89-b9dd-5bf67838ab1e

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