Form 483

Medartis Inc. Form 483, 2026-06-03

FDA issued a Form 483 to Medartis Inc. on 2026-06-03 with 3 public-safe observations.

483· Form 483 issuedMedical Devices & Rad Health3 observations

Medartis Inc. · Warsaw, United States · Issued June 3, 2026

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.

3 Jun 2026
ISO 13485:2016 Clause 8.1

Methods for monitoring, measurement, analysis, and improvement not determined

Cited by Suyang Qin

3 Jun 2026
ISO 13485:2016 Clause 8.2.1

Information gathered in feedback process not used as input into risk management

Cited by Suyang Qin

3 Jun 2026
ISO 13485:2016 Clause 8.4

Procedures for analysis of data not documented

Cited by Suyang Qin

Inspected site

MIMedartis Inc.Warsaw, United States

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
ISO 13485:2016 Clause 8.1Cited across public-safe Form 483 observations1x
ISO 13485:2016 Clause 8.2.1Cited across public-safe Form 483 observations1x
ISO 13485:2016 Clause 8.4Cited 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