Overview
- 4 FDA inspections are on record.
- 1 inspection produced a Form 483.
- The most recent recorded inspection date is 2025-02-06.
At a glance
Inspections
4
Form 483s
1
EIRs
0
Last outcome
Form 483
Inspection history
FDA inspections on record, most recent first.
| Inspection | Category | Outcome | Form 483 |
|---|---|---|---|
| 3 Feb 2025 – 6 Feb 2025 | Medical Devices & Rad Health | 483 | View 483 → |
| 17 Apr 2017 – 19 Apr 2017 | Medical Devices & Rad Health | Clean | |
| 29 Feb 2016 – 3 Mar 2016 | Medical Devices & Rad Health | Clean | |
| 13 Sep 2012 | Not recorded | Clean |
Observations on record
Form 483 observations cited at this site, most recent first.
6 Feb 2025
21 CFR 820.250(a)
Statistical techniques - Lack of or inadequate procedures
Cited by Dianiris C Ayala
Investigators
FDA investigators tied to this site in the record.
Recurring citations
CFR citation patterns observed across this site's inspections.
| Citation | What it covers | Cited |
|---|---|---|
| 21 CFR 820.198(d) | Cited across public-safe Form 483 observations | 1x |
| 21 CFR 820.250(a) | Cited across public-safe Form 483 observations | 1x |
Full site report
Get the verbatim findings behind Kaneka Corporation'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