Form 483

Keystone Industries Form 483, 2025-09-30

FDA issued a Form 483 to Keystone Industries on 2025-09-30 with 4 public-safe observations.

483· Form 483 issuedMedical Devices & Rad Health4 observations

Keystone Industries · Gibbstown, United States · Issued September 30, 2025

Overview

  • 4 public-safe observations are available for this inspection.
  • 4 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.

30 Sep 2025
21 CFR 820.198(a)

Lack of or inadequate complaint procedures

Cited by Shirley S Wen

30 Sep 2025
21 CFR 820.250(a)

Statistical techniques - Lack of or inadequate procedures

Cited by Shirley S Wen

30 Sep 2025
21 CFR 820.25(a)

Personnel

Cited by Shirley S Wen

30 Sep 2025
21 CFR 820.72(b)

Remedial action

Cited by Shirley S Wen

Inspected site

KIKeystone IndustriesGibbstown, United States

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 820.198(a)Cited across public-safe Form 483 observations1x
21 CFR 820.25(a)Cited across public-safe Form 483 observations1x
21 CFR 820.250(a)Cited across public-safe Form 483 observations1x
21 CFR 820.72(b)Cited across public-safe Form 483 observations1x

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