Form 483

Ventana Medical Systems, Inc. Form 483, 2026-02-10

FDA issued a Form 483 to Ventana Medical Systems, Inc. on 2026-02-10 with 2 public-safe observations.

483· Form 483 issuedMedical Devices & Rad Health2 observations

Ventana Medical Systems, Inc. · Tucson, United States · Issued February 10, 2026

Overview

  • 2 public-safe observations are available for this inspection.
  • 2 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.

10 Feb 2026
ISO 13485:2016 Clause 7.5.6

Planned results not consistently met during validation of processes

Cited by Scott D Stevens

10 Feb 2026
ISO 13485:2016 Clause 8.2.2

Correction or corrective action resulting from complaint handling not documented

Cited by Scott D Stevens

Inspected site

VMVentana Medical Systems, Inc.Tucson, United States

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
ISO 13485:2016 Clause 7.5.6Cited across public-safe Form 483 observations1x
ISO 13485:2016 Clause 8.2.2Cited across public-safe Form 483 observations1x

Source document

PDF
PDF available

Form 483 source document

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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