Form 483

Ventec Life Systems, Inc. Form 483, 2025-12-17

FDA issued a Form 483 to Ventec Life Systems, Inc. on 2025-12-17 with 4 public-safe observations.

483· Form 483 issuedMedical Devices & Rad Health4 observations

Ventec Life Systems, Inc. · Bothell, United States · Issued December 17, 2025

Overview

  • 4 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.

17 Dec 2025
21 CFR 820.184

DHR content

Cited by Brian R Hendricks

17 Dec 2025
21 CFR 820.184

DHR content

Cited by Brian R Hendricks

17 Dec 2025
21 CFR 820.198(a)

Lack of or inadequate complaint procedures

Cited by Brian R Hendricks

17 Dec 2025
21 CFR 820.198(a)

Lack of or inadequate complaint procedures

Cited by Brian R Hendricks

Inspected site

VLVentec Life Systems, Inc.Bothell, United States

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 820.184Cited across public-safe Form 483 observations2x
21 CFR 820.198(a)Cited across public-safe Form 483 observations2x

Source document

PDF
PDF available

Form 483 source document

The source document is available to authorized Atlas users.

Full 483 report

Get the verbatim text of all 4 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