Form 483

Agupunt USA Corp Form 483, 2026-03-25

FDA issued a Form 483 to Agupunt USA Corp on 2026-03-25 with 4 public-safe observations.

483· Form 483 issuedMedical Devices & Rad Health4 observations

Agupunt USA Corp · Miami, United States · Issued March 25, 2026

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.

25 Mar 2026
21 CFR 803.17(b)(1)

Info evaluated to determine if event was reportable

Cited by Ebony D Sanon

25 Mar 2026
21 CFR 803.17(b)(1)

Info evaluated to determine if event was reportable

Cited by Ebony D Sanon

25 Mar 2026
ISO 13485:2016 Clause 7.4.3

Purchased product verification activities not established or implemented

Cited by Ebony D Sanon

25 Mar 2026
ISO 13485:2016 Clause 7.4.3

Purchased product verification activities not established or implemented

Cited by Ebony D Sanon

Inspected site

AUAgupunt USA CorpMiami, United States

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 803.17(b)(1)Cited across public-safe Form 483 observations2x
ISO 13485:2016 Clause 7.4.3Cited across public-safe Form 483 observations2x

Full 483 report

Get the verbatim text of all 4 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