Form 483

PLEXUS Manufacturing Sdn. Bhd. Form 483, 2022-11-11

FDA issued a Form 483 to PLEXUS Manufacturing Sdn. Bhd. on 2022-11-11 with 2 public-safe observations.

483· Form 483 issuedMedical Devices & Rad Health2 observations

PLEXUS Manufacturing Sdn. Bhd. · Bayan Lepas, Malaysia · Issued November 11, 2022

Overview

  • 2 public-safe observations are available for this inspection.
  • 2 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.

11 Nov 2022
21 CFR 820.184

DHR content

Cited by Thai T Duong

11 Nov 2022
21 CFR 820.70(a)

Process control procedures, Lack of or inadequate procedures

Cited by Thai T Duong

Inspected site

PMPLEXUS Manufacturing Sdn. Bhd.Bayan Lepas, Malaysia

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 820.70(a)Cited across public-safe Form 483 observations1x

Full 483 report

Get the verbatim text of all 2 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