# FDA Inspection 1322038 - Joylux, Inc. - June 15, 2026

Source: https://www.keypedia.com/records/fda_inspections/joylux-inc/2d006a77-205d-4d46-a3f1-1ea524a10136
Source feed: FDA_Inspections

> FDA Inspection 1322038 for Joylux, Inc. on June 15, 2026. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1322038
- Company Name: Joylux, Inc.
- Inspection Date: 2026-06-15
- 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 1322038 - 2026-06-15](https://www.keypedia.com/records/fda_inspections/joylux-inc/6d8efcb4-a4bf-4a78-ba0d-f32b7ba8fa8f)

Company: https://www.keypedia.com/companies/joylux-inc/7149caf0-247d-4563-be75-c05557bd79b0

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