Form 483

Medicore Co., Ltd. Form 483, 2023-11-09

FDA issued a Form 483 to Medicore Co., Ltd. on 2023-11-09 with 5 public-safe observations.

483· Form 483 issuedMedical Devices & Rad Health5 observations

Medicore Co., Ltd. · Seongnam, Korea (the Republic of) · Issued November 9, 2023

Overview

  • 5 public-safe observations are available for this inspection.
  • 5 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.

9 Nov 2023
21 CFR 820.184

Lack of or inadequate DHR procedures

Cited by Daniel J Lahar

9 Nov 2023
21 CFR 820.198(b)

Review and evaluation for investigation

Cited by Daniel J Lahar

9 Nov 2023
21 CFR 820.25(b)

Training - Lack of or inadequate procedures

Cited by Daniel J Lahar

9 Nov 2023
21 CFR 820.80(a)

Lack of or inadequate procedures - Acceptance activities

Cited by Daniel J Lahar

9 Nov 2023
21 CFR 820.90(a)

Nonconforming product, Lack of or inadequate procedures

Cited by Daniel J Lahar

Inspected site

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

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 820.184Cited across public-safe Form 483 observations1x
21 CFR 820.198(b)Cited across public-safe Form 483 observations1x
21 CFR 820.25(b)Cited across public-safe Form 483 observations1x
21 CFR 820.80(a)Cited across public-safe Form 483 observations1x
21 CFR 820.90(a)Cited across public-safe Form 483 observations1x

Source document

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Form 483 source document

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Full 483 report

Get the verbatim text of all 5 observations

The source PDF, 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