Form 483

Vassen Co. Ltd. Form 483, 2026-05-14

FDA issued a Form 483 to Vassen Co. Ltd. on 2026-05-14 with 4 public-safe observations.

483· Form 483 issuedMedical Devices & Rad Health4 observations

Vassen Co. Ltd. · Pyeongtaek, Korea (the Republic of) · Issued May 14, 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.

14 May 2026
21 CFR 803.17

Lack of Written MDR Procedures

Cited by Esteban Beltran

14 May 2026
ISO 13485:2016 Clause 4.1.2

Risk-based approach not applied to QMS processes

Cited by Esteban Beltran

14 May 2026
ISO 13485:2016 Clause 4.1.5

Inadequate monitoring and control over outsourced processes

Cited by Esteban Beltran

14 May 2026
ISO 13485:2016 Clause 7.3.9

Procedures to control design and development changes not documented

Cited by Esteban Beltran

Inspected site

VCVassen Co. Ltd.Pyeongtaek, Korea (the Republic of)

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 803.17Cited across public-safe Form 483 observations1x
ISO 13485:2016 Clause 4.1.2Cited across public-safe Form 483 observations1x
ISO 13485:2016 Clause 4.1.5Cited across public-safe Form 483 observations1x
ISO 13485:2016 Clause 7.3.9Cited 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