Form 483

CGR Products MN, LLC. Form 483, 2026-03-12

FDA issued a Form 483 to CGR Products MN, LLC. on 2026-03-12 with 3 public-safe observations.

483· Form 483 issuedMedical Devices & Rad Health3 observations

CGR Products MN, LLC. · Inver Grove Heights, United States · Issued March 12, 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.

12 Mar 2026
ISO 13485:2016 Clause 7.5.1

Production controls not adequate

Cited by Albert L Nguyen

12 Mar 2026
ISO 13485:2016 Clause 8.3.1

Records of nonconforming product and actions taken not maintained

Cited by Albert L Nguyen

12 Mar 2026
ISO 13485:2016 Clause 8.5.2

Corrective action procedures not documented

Cited by Albert L Nguyen

Inspected site

CPCGR Products MN, LLC.Inver Grove Heights, United States

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
ISO 13485:2016 Clause 7.5.1Cited across public-safe Form 483 observations1x
ISO 13485:2016 Clause 8.3.1Cited across public-safe Form 483 observations1x
ISO 13485:2016 Clause 8.5.2Cited 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