Form 483

Dongguan Jianwei Electronics Products Co., Ltd. Form 483, 2014-06-05

FDA issued a Form 483 to Dongguan Jianwei Electronics Products Co., Ltd. on 2014-06-05 with 10 public-safe observations.

483· Form 483 issuedMedical Devices & Rad Health10 observations

Dongguan Jianwei Electronics Products Co., Ltd. · Dongguan City, China · Issued June 5, 2014

Overview

  • 10 public-safe observations are available for this inspection.
  • 10 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.

5 Jun 2014
21 CFR 820.22

Quality audits - Lack of or inadequate procedures

Cited by Catherine J Laufmann

5 Jun 2014
21 CFR 820.30(f)

Design verification - Lack of or inadequate procedures

Cited by Catherine J Laufmann

5 Jun 2014
21 CFR 820.50

Purchasing controls, Lack of or inadequate procedures

Cited by Catherine J Laufmann

5 Jun 2014
21 CFR 820.70(i)

Software validation for automated processes

Cited by Catherine J Laufmann

5 Jun 2014
21 CFR 820.72(a)

Equipment control activity documentation

Cited by Catherine J Laufmann

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 820.198(a)Cited across public-safe Form 483 observations1x
21 CFR 820.22Cited across public-safe Form 483 observations1x
21 CFR 820.250(a)Cited across public-safe Form 483 observations1x
21 CFR 820.30(f)Cited across public-safe Form 483 observations1x
21 CFR 820.50Cited across public-safe Form 483 observations1x
21 CFR 820.70(i)Cited across public-safe Form 483 observations1x
21 CFR 820.72(a)Cited across public-safe Form 483 observations1x
21 CFR 820.75(a)Cited across public-safe Form 483 observations1x
21 CFR 820.90(b)(2)Cited across public-safe Form 483 observations1x

Full 483 report

Get the verbatim text of all 10 observations

Every observation in full, 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