Overview
- 6 FDA inspections are on record.
- 4 inspections produced a Form 483.
- The most recent recorded inspection date is 2024-11-14.
At a glance
Inspections
6
Form 483s
4
EIRs
0
Last outcome
Clean
Inspection history
FDA inspections on record, most recent first.
| Inspection | Category | Outcome | Form 483 |
|---|---|---|---|
| 12 Nov 2024 – 14 Nov 2024 | Medical Devices & Rad Health | Clean | |
| 7 Nov 2022 – 9 Nov 2022 | Medical Devices & Rad Health | 483 | View 483 → |
| 11 Dec 2019 – 13 Dec 2019 | Medical Devices & Rad Health | 483 | View 483 → |
| 29 Apr 2015 – 5 May 2015 | Medical Devices & Rad Health | 483 | View 483 → |
| 27 Oct 2011 | Not recorded | Clean | |
| 29 Jun 2010 | Not recorded | 483 | View 483 → |
Observations on record
Form 483 observations cited at this site, most recent first.
9 Nov 2022
21 CFR 820.30(g)
Design validation- Lack of or inadequate procedures
Cited by Stanley B Eugene
9 Nov 2022
21 CFR 820.30(g)
Design validation- Lack of or inadequate procedures
Cited by Stanley B Eugene
Investigators
FDA investigators tied to this site in the record.
Karen M Rodriguez2 insp.
Matthew T Sanchez1 insp.
Stanley B Eugene1 insp.
Althea A Williams1 insp.
Richard K Vogel1 insp.
Recurring citations
CFR citation patterns observed across this site's inspections.
| Citation | What it covers | Cited |
|---|---|---|
| 21 CFR 820.30(g) | Cited across public-safe Form 483 observations | 7x |
| 21 CFR 820.198(a) | Cited across public-safe Form 483 observations | 6x |
| 21 CFR 820.40 | Cited across public-safe Form 483 observations | 6x |
| 21 CFR 820.100(a) | Cited across public-safe Form 483 observations | 4x |
| 21 CFR 820.50 | Cited across public-safe Form 483 observations | 2x |
| 21 CFR 820.22 | Cited across public-safe Form 483 observations | 1x |
| 21 CFR 820.30(c) | Cited across public-safe Form 483 observations | 1x |
| 21 CFR 820.50(a) | Cited across public-safe Form 483 observations | 1x |
Full site report
Get the verbatim findings behind LD Technology, LLC'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