Overview
- 5 FDA inspections are on record.
- 4 inspections produced a Form 483.
- The most recent recorded inspection date is 2026-05-15.
At a glance
Inspections
5
Form 483s
4
EIRs
0
Last outcome
Form 483
Inspection history
FDA inspections on record, most recent first.
| Inspection | Category | Outcome | Form 483 |
|---|---|---|---|
| 11 May 2026 – 15 May 2026 | Human Drugs | 483 | View 483 → |
| 6 Feb 2023 – 9 Feb 2023 | Medical Devices & Rad Health | Clean | |
| 9 Sep 2019 – 13 Sep 2019 | Human Drugs | 483 | On file |
| 5 Nov 2018 – 9 Nov 2018 | Human Drugs | 483 | On file |
| 24 Jul 2017 – 2 Aug 2017 | Human Drugs | 483 | View 483 → |
Observations on record
Form 483 observations cited at this site, most recent first.
15 May 2026
21 CFR 212.71(a)
Procedures to Investigate Cause of Non-Conforming Product
Cited by Shelby N Turner
Investigators
FDA investigators tied to this site in the record.
Shelby N Turner1 insp.
Iris C Macinnes1 insp.
Margaret M Annes1 insp.
Kenitra D Hewitt1 insp.
Shanna N Purdy1 insp.
Jason R Caballero1 insp.
Reba A Gates1 insp.
Hala L Selby1 insp.
Recurring citations
CFR citation patterns observed across this site's inspections.
| Citation | What it covers | Cited |
|---|---|---|
| 21 CFR 212.20(b) | Cited across public-safe Form 483 observations | 1x |
| 21 CFR 212.30(a) | Cited across public-safe Form 483 observations | 1x |
| 21 CFR 212.60(b) | Cited across public-safe Form 483 observations | 1x |
| 21 CFR 212.60(g)(3) | Cited across public-safe Form 483 observations | 1x |
| 21 CFR 212.71(a) | Cited across public-safe Form 483 observations | 1x |
| 21 CFR 212.71(b) | Cited across public-safe Form 483 observations | 1x |
Full site report
Get the verbatim findings behind this site's 4 Form 483s
Source PDFs 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