FDA-Inspected Site

Labone, LLC.

5 FDA inspections are on record for Labone, LLC. in Lenexa, United States.

Clean· No action indicated

Lenexa, United States · Last updated July 10, 2026

Overview

  • 5 FDA inspections are on record.
  • 1 inspection produced a Form 483.
  • The most recent recorded inspection date is 2025-10-15.

At a glance

Inspections

5

Form 483s

1

EIRs

0

Last outcome

Clean

Inspection history

FDA inspections on record, most recent first.

InspectionCategoryOutcomeForm 483
14 Oct 2025 – 15 Oct 2025Medical Devices & Rad HealthClean
23 Jan 2023 – 25 Jan 2023Medical Devices & Rad HealthClean
27 Nov 2018 – 30 Nov 2018Medical Devices & Rad Health483View 483 →
20 May 2015 – 22 May 2015Medical Devices & Rad HealthClean
14 Sep 2010Not recordedClean

Observations on record

Form 483 observations cited at this site, most recent first.

30 Nov 2018
21 CFR 820.100(a)

Lack of or inadequate procedures

Cited by Eric C Fox

30 Nov 2018
21 CFR 820.100(a)

Lack of or inadequate procedures

Cited by Eric C Fox

Investigators

FDA investigators tied to this site in the record.

Recurring citations

CFR citation patterns observed across this site's inspections.

CitationWhat it coversCited
21 CFR 820.100(a)Cited across public-safe Form 483 observations2x

Full site report

Get the verbatim findings behind Labone, LLC.'s 1 Form 483

Source PDFs, verbatim observations, and recurring CFR citations, so your team knows what this site gets cited for.

  • The site's full inspection history, with every Form 483 and its outcome
  • Warning letters and recalls tied to the company behind it
  • Whether recurring CFR citations get closed out or repeat