Form 483

Vee International Inc. Form 483, 2026-05-18

FDA issued a Form 483 to Vee International Inc. on 2026-05-18 with 4 public-safe observations.

483· Form 483 issuedMedical Devices & Rad Health4 observations

Vee International Inc. · Garden City, United States · Issued May 18, 2026

Overview

  • 4 public-safe observations are available for this inspection.
  • 4 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.

18 May 2026
21 CFR 801.40(a)

Form of a unique device identifier

Cited by Andrew J Garufi

18 May 2026
ISO 13485:2016 Clause 4.1.5

Control over outsourced processes not proportionate to risk

Cited by Andrew J Garufi

18 May 2026
ISO 13485:2016 Clause 5.6.1

Management review procedures not documented

Cited by Andrew J Garufi

18 May 2026
ISO 13485:2016 Clause 8.2.4

Internal audits not conducted to ensure QMS meets requirements and is effective

Cited by Andrew J Garufi

Inspected site

VIVee International Inc.Garden City, United States

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 801.40(a)Cited across public-safe Form 483 observations1x
ISO 13485:2016 Clause 4.1.5Cited across public-safe Form 483 observations1x
ISO 13485:2016 Clause 5.6.1Cited across public-safe Form 483 observations1x
ISO 13485:2016 Clause 8.2.4Cited across public-safe Form 483 observations1x

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