Form 483

Altor Safety Form 483, 2026-03-12

FDA issued a Form 483 to Altor Safety on 2026-03-12 with 10 public-safe observations.

483· Form 483 issuedMedical Devices & Rad Health10 observations

Altor Safety · Valley Cottage, United States · Issued March 12, 2026

Overview

  • 10 public-safe observations are available for this inspection.
  • 5 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
21 CFR 803.17

Lack of Written MDR Procedures

Cited by Andrew J Garufi

12 Mar 2026
21 CFR 803.17

Lack of Written MDR Procedures

Cited by Andrew J Garufi

12 Mar 2026
ISO 13485:2016 Clause 4.1.1

QMS not documented and maintained adequately

Cited by Andrew J Garufi

12 Mar 2026
ISO 13485:2016 Clause 4.1.1

QMS not documented and maintained adequately

Cited by Andrew J Garufi

12 Mar 2026
ISO 13485:2016 Clause 4.2.3

Medical device file not established and maintained

Cited by Andrew J Garufi

Inspected site

ASAltor SafetyValley Cottage, United States

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 803.17Cited across public-safe Form 483 observations2x
ISO 13485:2016 Clause 4.1.1Cited across public-safe Form 483 observations2x
ISO 13485:2016 Clause 4.2.3Cited across public-safe Form 483 observations2x
ISO 13485:2016 Clause 7.3.10Cited across public-safe Form 483 observations2x
ISO 13485:2016 Clause 7.5.6Cited across public-safe Form 483 observations2x

Full 483 report

Get the verbatim text of all 10 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