Joylux, Inc. – FDA Inspection, Jun 15, 2026

Record Details

This FDA Inspection record concerns Joylux, Inc., with an inspection on June 15, 2026, issued by the Center for Devices and Radiological Health, covering devices.

Company: Joylux, Inc.
Inspection Date: June 15, 2026
Product Type: Devices
Office: Center for Devices and Radiological Health
Person: Brian R. Hendricks (Investigator)

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ID · 6d8efcb4-a4bf-4a78-ba0d-f32b7ba8fa8f

Inspection Facts

Voluntary Action Indicated (VAI)

Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.

Inspection number: 1322038
Project area: Compliance: Devices

FDA Citations

21 CFR 801(a)Form of a unique device identifier
ISO 13485:2016 Clause 8.2.2Complaint handling procedures not documented
21 CFR 801.40(a)Form of a unique device identifier

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FDA Inspection

Joylux, Inc.June 15, 2026