Overview
- 5 FDA inspections are on record.
- 1 inspection produced a Form 483.
- The most recent recorded inspection date is 2024-09-12.
At a glance
Inspections
5
Form 483s
1
EIRs
0
Last outcome
Clean
Inspection history
FDA inspections on record, most recent first.
| Inspection | Category | Outcome | Form 483 |
|---|---|---|---|
| 9 Sep 2024 – 12 Sep 2024 | Medical Devices & Rad Health | Clean | |
| 27 Jan 2020 – 28 Jan 2020 | Medical Devices & Rad Health | Clean | |
| 12 Oct 2015 – 14 Oct 2015 | Medical Devices & Rad Health | Clean | |
| 18 Mar 2013 – 22 Mar 2013 | Medical Devices & Rad Health | Clean | |
| 12 Apr 2012 | Not recorded | WL | On file |
Observations on record
Form 483 observations cited at this site, most recent first.
12 Apr 2012
21 CFR 820.70(a)
Process control procedures, Lack of or inadequate procedures
Cited by Stephen D Eich
Investigators
FDA investigators tied to this site in the record.
Edward D Mcdonald1 insp.
Daniel J Lahar1 insp.
Stanley B Eugene1 insp.
Charles L Larson1 insp.
Sean T Creighton1 insp.
Stephen D Eich1 insp.
Recurring citations
CFR citation patterns observed across this site's inspections.
| Citation | What it covers | Cited |
|---|---|---|
| 21 CFR 820.70(a) | Cited across public-safe Form 483 observations | 2x |
| 21 CFR 820.100(a) | Cited across public-safe Form 483 observations | 1x |
| 21 CFR 820.75(a) | Cited across public-safe Form 483 observations | 1x |
Full site report
Get the verbatim findings behind Arriol International Corp.'s 1 Form 483
Source PDFs, verbatim observations, and 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