Overview
- 7 FDA inspections are on record.
- 4 inspections produced a Form 483.
- The most recent recorded inspection date is 2025-08-27.
At a glance
Inspections
7
Form 483s
4
EIRs
0
Last outcome
Form 483
Inspection history
FDA inspections on record, most recent first.
| Inspection | Category | Outcome | Form 483 |
|---|---|---|---|
| 25 Aug 2025 – 27 Aug 2025 | Medical Devices & Rad Health | 483 | View 483 → |
| 12 Sep 2022 – 16 Sep 2022 | Medical Devices & Rad Health | Clean | |
| 5 Jul 2017 – 12 Jul 2017 | Medical Devices & Rad Health | Clean | |
| 17 Jul 2015 – 7 Aug 2015 | Medical Devices & Rad Health | 483 | On file |
| 7 Oct 2014 – 21 Oct 2014 | Medical Devices & Rad Health | 483 | View 483 → |
| 6 Oct 2010 | Not recorded | 483 | View 483 → |
| 6 Dec 2006 | Not recorded | Clean |
Observations on record
Form 483 observations cited at this site, most recent first.
27 Aug 2025
21 CFR 820.90(a)
Nonconforming product, Lack of or inadequate procedures
Cited by Shuana H Xiong
21 Oct 2014
21 CFR 820.40(a)
Document review, approval by designated individual
Cited by Michelle J Glembin, Rafael A Kaup
21 Oct 2014
21 CFR 820.80(b)
Lack of or inadequate receiving acceptance procedures
Cited by Michelle J Glembin, Rafael A Kaup
21 Oct 2014
21 CFR 820.90(a)
Nonconforming product, Lack of or inadequate procedures
Cited by Michelle J Glembin, Rafael A Kaup
21 Oct 2014
21 CFR 820.100(a)
Lack of or inadequate procedures
Cited by Michelle J Glembin, Rafael A Kaup
Investigators
FDA investigators tied to this site in the record.
Richard J Tucker2 insp.
Michelle J Glembin2 insp.
Shuana H Xiong1 insp.
Tyler R Courtney1 insp.
Rafael A Kaup1 insp.
Melissa J Holz1 insp.
Recurring citations
CFR citation patterns observed across this site's inspections.
| Citation | What it covers | Cited |
|---|---|---|
| 21 CFR 820.181 | Cited across public-safe Form 483 observations | 2x |
| 21 CFR 820.80(b) | Cited across public-safe Form 483 observations | 2x |
| 21 CFR 820.90(a) | Cited across public-safe Form 483 observations | 2x |
| 21 CFR 820.100(a) | Cited across public-safe Form 483 observations | 1x |
| 21 CFR 820.184 | Cited across public-safe Form 483 observations | 1x |
| 21 CFR 820.198(b) | Cited across public-safe Form 483 observations | 1x |
| 21 CFR 820.22 | Cited across public-safe Form 483 observations | 1x |
| 21 CFR 820.30(h) | Cited across public-safe Form 483 observations | 1x |
| 21 CFR 820.40(a) | Cited across public-safe Form 483 observations | 1x |
| 21 CFR 820.80(d) | Cited across public-safe Form 483 observations | 1x |
| 21 CFR 820.90(b)(1) | Cited across public-safe Form 483 observations | 1x |
| 21 CFR 820.90(b)(2) | Cited across public-safe Form 483 observations | 1x |
Full site report
Get the verbatim findings behind TreyMed, Inc.'s 4 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