Form 483

Dongguan Bao Kang Dian Zi Ke Ji Ltd. Form 483, 2017-06-08

FDA issued a Form 483 to Dongguan Bao Kang Dian Zi Ke Ji Ltd. on 2017-06-08 with 1 public-safe observation.

483· Form 483 issuedMedical Devices & Rad Health1 observation

Dongguan Bao Kang Dian Zi Ke Ji Ltd. · Guangdong, China · Issued June 8, 2017

Overview

  • 1 public-safe observation is available for this inspection.
  • 1 structured CFR citation is represented.
  • 1 investigator is tied to this Form 483.

Inspectional observations

Each observation cites the regulation FDA found the firm out of compliance with.

8 Jun 2017
21 CFR 820.120(b)

DHR documentation of label release {see also 820.184}

Cited by Kwong P Lee

Inspected site

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 820.120(b)Cited across public-safe Form 483 observations1x

Full 483 report

Get the verbatim text of all 1 observation

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