Form 483

Magnamed Tecnologia Medica S/A Form 483, 2025-04-10

FDA issued a Form 483 to Magnamed Tecnologia Medica S/A on 2025-04-10 with 8 public-safe observations.

483· Form 483 issuedMedical Devices & Rad Health8 observations

Magnamed Tecnologia Medica S/A · Cotia, Brazil · Issued April 10, 2025

Overview

  • 8 public-safe observations are available for this inspection.
  • 8 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 Apr 2025
21 CFR 801.20(a)

Label to bear a unique device identifier

Cited by Colin E Tack

10 Apr 2025
21 CFR 820.184

Lack of or inadequate DHR procedures

Cited by Colin E Tack

10 Apr 2025
21 CFR 820.198(a)

Lack of or inadequate complaint procedures

Cited by Colin E Tack

10 Apr 2025
21 CFR 820.250(b)

Sampling plans

Cited by Colin E Tack

10 Apr 2025
21 CFR 820.30(g)

Design validation- Lack of or inadequate procedures

Cited by Colin E Tack

Inspected site

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 801.20(a)Cited across public-safe Form 483 observations1x
21 CFR 820.184Cited across public-safe Form 483 observations1x
21 CFR 820.198(a)Cited across public-safe Form 483 observations1x
21 CFR 820.250(b)Cited across public-safe Form 483 observations1x
21 CFR 820.30(g)Cited across public-safe Form 483 observations1x
21 CFR 820.30(i)Cited across public-safe Form 483 observations1x
21 CFR 820.50Cited across public-safe Form 483 observations1x
21 CFR 820.75(a)Cited across public-safe Form 483 observations1x

Full 483 report

Get the verbatim text of all 8 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