Form 483

KANEKA MEDICAL VIETNAM Co.,Ltd. Form 483, 2025-02-13

FDA issued a Form 483 to KANEKA MEDICAL VIETNAM Co.,Ltd. on 2025-02-13 with 3 public-safe observations.

483· Form 483 issuedMedical Devices & Rad Health3 observations

KANEKA MEDICAL VIETNAM Co.,Ltd. · Thuan An, Vietnam · Issued February 13, 2025

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.

13 Feb 2025
21 CFR 820.100(a)

Lack of or inadequate procedures

Cited by Dianiris C Ayala

13 Feb 2025
21 CFR 820.250(a)

Statistical techniques - Lack of or inadequate procedures

Cited by Dianiris C Ayala

13 Feb 2025
21 CFR 820.70(a)

Production processes

Cited by Dianiris C Ayala

Inspected site

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 820.100(a)Cited across public-safe Form 483 observations1x
21 CFR 820.250(a)Cited across public-safe Form 483 observations1x
21 CFR 820.70(a)Cited 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