Form 483

Joylux, Inc. Form 483, 2026-06-15

FDA issued a Form 483 to Joylux, Inc. on 2026-06-15 with 4 public-safe observations.

483· Form 483 issuedMedical Devices & Rad Health4 observations

Joylux, Inc. · Seattle, United States · Issued June 15, 2026

Overview

  • 4 public-safe observations are available for this inspection.
  • 2 structured CFR citations are represented.
  • 1 investigator is tied to this Form 483.

Inspectional observations

Each observation cites the regulation FDA found the firm out of compliance with.

15 Jun 2026
21 CFR 801.40(a)

Form of a unique device identifier

Cited by Brian R Hendricks

15 Jun 2026
21 CFR 801.40(a)

Form of a unique device identifier

Cited by Brian R Hendricks

15 Jun 2026
ISO 13485:2016 Clause 8.2.2

Complaint handling procedures not documented

Cited by Brian R Hendricks

15 Jun 2026
ISO 13485:2016 Clause 8.2.2

Complaint handling procedures not documented

Cited by Brian R Hendricks

Inspected site

JIJoylux, Inc.Seattle, United States

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 801.40(a)Cited across public-safe Form 483 observations2x
ISO 13485:2016 Clause 8.2.2Cited across public-safe Form 483 observations2x

Full 483 report

Get the verbatim text of all 4 observations

The full inspection record, as Atlas holds it, so your team sees exactly what was cited and how it was answered.

  • The site's full inspection history around this Form 483
  • Whether these citations escalated to a warning letter
  • The investigators involved and the citations they repeat elsewhere