Form 483

Medicore Co., Ltd. Form 483, 2026-05-20

FDA issued a Form 483 to Medicore Co., Ltd. on 2026-05-20 with 3 public-safe observations.

483· Form 483 issuedMedical Devices & Rad Health3 observations

Medicore Co., Ltd. · Seongnam, Korea (the Republic of) · Issued May 20, 2026

Overview

  • 3 public-safe observations are available for this inspection.
  • 3 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.

20 May 2026
ISO 13485:2016 Clause 7.4.3

Purchased product verification activities not established or implemented

Cited by Esteban Beltran

20 May 2026
ISO 13485:2016 Clause 8.2.4

Objectivity and impartiality of internal audit process not ensured

Cited by Esteban Beltran

20 May 2026
ISO 13485:2016 Clause 8.5.2

Corrective action procedures not documented

Cited by Esteban Beltran

Inspected site

MCMedicore Co., Ltd.Seongnam, Korea (the Republic of)

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
ISO 13485:2016 Clause 7.4.3Cited across public-safe Form 483 observations1x
ISO 13485:2016 Clause 8.2.4Cited across public-safe Form 483 observations1x
ISO 13485:2016 Clause 8.5.2Cited across public-safe Form 483 observations1x

Full 483 report

Get the verbatim text of all 3 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