Overview
- 2 FDA inspections are on record.
- 1 inspection produced a Form 483.
- The most recent recorded inspection date is 2017-06-08.
At a glance
Inspections
2
Form 483s
1
EIRs
0
Last outcome
Form 483
Inspection history
FDA inspections on record, most recent first.
| Inspection | Category | Outcome | Form 483 |
|---|---|---|---|
| 5 Jun 2017 – 8 Jun 2017 | Medical Devices & Rad Health | 483 | View 483 → |
| 21 Apr 2014 – 24 Apr 2014 | Medical Devices & Rad Health | Clean |
Observations on record
Form 483 observations cited at this site, most recent first.
8 Jun 2017
21 CFR 820.120(b)
DHR documentation of label release {see also 820.184}
Cited by Kwong P Lee
Investigators
FDA investigators tied to this site in the record.
Kwong P Lee1 insp.
Allison M Mcgloin1 insp.
Recurring citations
CFR citation patterns observed across this site's inspections.
| Citation | What it covers | Cited |
|---|---|---|
| 21 CFR 820.120(b) | Cited across public-safe Form 483 observations | 1x |
Full site report
Get the verbatim findings behind Dongguan Bao Kang Dian Zi Ke Ji Ltd.'s 1 Form 483
Recurring CFR citations, so your team knows what this site gets cited for.
- The site's full inspection history, with every Form 483 and its outcome
- Warning letters and recalls tied to the company behind it
- Whether recurring CFR citations get closed out or repeat