Form 483

Innovize LLC Form 483, 2025-03-26

FDA issued a Form 483 to Innovize LLC on 2025-03-26 with 4 public-safe observations.

483· Form 483 issuedMedical Devices & Rad Health4 observations

Innovize LLC · Saint Paul, United States · Issued March 26, 2025

Overview

  • 4 public-safe observations are available for this inspection.
  • 2 structured CFR citations are represented.
  • 2 investigators are tied to this Form 483.

Inspectional observations

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

26 Mar 2025
21 CFR 820.198(e)

Records of complaint investigation

Cited by Susan M Matthias, Alicia U Jacobo

26 Mar 2025
21 CFR 820.198(e)

Records of complaint investigation

Cited by Susan M Matthias, Alicia U Jacobo

26 Mar 2025
21 CFR 820.40(a)

Document review, approval by designated individual

Cited by Susan M Matthias, Alicia U Jacobo

26 Mar 2025
21 CFR 820.40(a)

Document review, approval by designated individual

Cited by Susan M Matthias, Alicia U Jacobo

Inspected site

ILInnovize LLCSaint Paul, United States

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 820.198(e)Cited across public-safe Form 483 observations2x
21 CFR 820.40(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