Form 483

MAXSTAR Industrial Co., Ltd. Form 483, 2023-02-09

FDA issued a Form 483 to MAXSTAR Industrial Co., Ltd. on 2023-02-09 with 5 public-safe observations.

483· Form 483 issuedMedical Devices & Rad Health5 observations

MAXSTAR Industrial Co., Ltd. · Gimpo, Korea (the Republic of) · Issued February 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 Feb 2023
21 CFR 820.30(b)

Design plans- updated

Cited by Kelvin Cheung

9 Feb 2023
21 CFR 820.30(g)

Design validation - production units

Cited by Kelvin Cheung

9 Feb 2023
21 CFR 820.50(a)(1)

Documented evaluation

Cited by Kelvin Cheung

9 Feb 2023
21 CFR 820.75(c)

Process changes - review, evaluation and revalidation

Cited by Kelvin Cheung

9 Feb 2023
21 CFR 820.80(b)

Incoming acceptance records, documentation

Cited by Kelvin Cheung

Inspected site

MIMAXSTAR Industrial Co., Ltd.Gimpo, Korea (the Republic of)

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 820.30(b)Cited across public-safe Form 483 observations1x
21 CFR 820.30(g)Cited across public-safe Form 483 observations1x
21 CFR 820.50(a)(1)Cited across public-safe Form 483 observations1x
21 CFR 820.75(c)Cited across public-safe Form 483 observations1x
21 CFR 820.80(b)Cited across public-safe Form 483 observations1x

Full 483 report

Get the verbatim text of all 5 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