Form 483

Medline Industries, LP Form 483, 2026-02-06

FDA issued a Form 483 to Medline Industries, LP on 2026-02-06 with 2 public-safe observations.

483· Form 483 issuedMedical Devices & Rad Health2 observations

Medline Industries, LP · Arlington Heights, United States · Issued February 6, 2026

Overview

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

Inspectional observations

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

6 Feb 2026
ISO 13485:2016 Clause 8.3.1

Nonconforming product not adequately evaluated

Cited by Chad E Schmear

6 Feb 2026
ISO 13485:2016 Clause 8.3.1

Nonconforming product not identified and controlled

Cited by Chad E Schmear

Inspected site

MIMedline Industries, LPArlington Heights, United States

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
ISO 13485:2016 Clause 8.3.1Cited across public-safe Form 483 observations2x

Source document

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PDF available

Form 483 source document

The source document is available to authorized Atlas users.

Full 483 report

Get the verbatim text of all 2 observations

The source PDF, 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