Form 483

Aptyx Charlotte, LLC Form 483, 2025-12-15

FDA issued a Form 483 to Aptyx Charlotte, LLC on 2025-12-15 with 3 public-safe observations.

483· Form 483 issuedMedical Devices & Rad Health3 observations

Aptyx Charlotte, LLC · Charlotte, United States · Issued December 15, 2025

Overview

  • 3 public-safe observations are available for this inspection.
  • 3 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 Dec 2025
21 CFR 820.30(e)

Design review - documentation

Cited by Gamal A Norton

15 Dec 2025
21 CFR 820.30(h)

Design transfer - Lack of or inadequate procedures

Cited by Gamal A Norton

15 Dec 2025
21 CFR 820.75(a)

Lack of or inadequate process validation

Cited by Gamal A Norton

Inspected site

ACAptyx Charlotte, LLCCharlotte, United States

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 820.30(e)Cited across public-safe Form 483 observations1x
21 CFR 820.30(h)Cited across public-safe Form 483 observations1x
21 CFR 820.75(a)Cited across public-safe Form 483 observations1x

Full 483 report

Get the verbatim text of all 3 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