Overview
- 6 FDA inspections are on record.
- 3 inspections produced a Form 483.
- The most recent recorded inspection date is 2019-08-29.
At a glance
Inspections
6
Form 483s
3
EIRs
0
Last outcome
Form 483
Inspection history
FDA inspections on record, most recent first.
| Inspection | Category | Outcome | Form 483 |
|---|---|---|---|
| 27 Aug 2019 – 29 Aug 2019 | Medical Devices & Rad Health | 483 | View 483 → |
| 14 Oct 2015 – 16 Oct 2015 | Medical Devices & Rad Health | 483 | On file |
| 28 Nov 2011 | Not recorded | Clean | |
| 28 Jan 2009 | Not recorded | 483 | On file |
| 8 Feb 2005 | Not recorded | Clean | |
| 12 Jun 2003 | Not recorded | Clean |
Observations on record
Form 483 observations cited at this site, most recent first.
29 Aug 2019
21 CFR 820.50
Purchasing controls, Lack of or inadequate procedures
Cited by Matthew M Vernon
29 Aug 2019
21 CFR 820.50
Purchasing controls, Lack of or inadequate procedures
Cited by Matthew M Vernon
29 Aug 2019
21 CFR 820.90(a)
Nonconforming product, Lack of or inadequate procedures
Cited by Matthew M Vernon
29 Aug 2019
21 CFR 820.90(a)
Nonconforming product, Lack of or inadequate procedures
Cited by Matthew M Vernon
29 Aug 2019
21 CFR 820.90(a)
Nonconforming product, Lack of or inadequate procedures
Cited by Matthew M Vernon
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 820.90(a) | Cited across public-safe Form 483 observations | 4x |
| 21 CFR 820.50 | Cited across public-safe Form 483 observations | 2x |
Full site report
Get the verbatim findings behind ARP Manufacturing's 3 Form 483s
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