Overview
- 2 FDA inspections are on record.
- 2 inspections produced a Form 483.
- The most recent recorded inspection date is 2025-10-16.
At a glance
Inspections
2
Form 483s
2
EIRs
0
Last outcome
Form 483
Inspection history
FDA inspections on record, most recent first.
| Inspection | Category | Outcome | Form 483 |
|---|---|---|---|
| 14 Oct 2025 – 16 Oct 2025 | Medical Devices & Rad Health | 483 | View 483 → |
| 4 Jan 2023 – 5 Jan 2023 | Medical Devices & Rad Health | 483 | View 483 → |
Observations on record
Form 483 observations cited at this site, most recent first.
16 Oct 2025
21 CFR 820.30(i)
Design changes - Lack of or Inadequate Procedures
Cited by Marvin A Marenco
5 Jan 2023
21 CFR 820.20(c)
Management review - defined interval, sufficient frequency
Cited by Ronald Ifraimov
Investigators
FDA investigators tied to this site in the record.
Marvin A Marenco1 insp.
Ronald Ifraimov1 insp.
Recurring citations
CFR citation patterns observed across this site's inspections.
| Citation | What it covers | Cited |
|---|---|---|
| 21 CFR 803.50(a)(2) | Cited across public-safe Form 483 observations | 1x |
| 21 CFR 820.198(a) | Cited across public-safe Form 483 observations | 1x |
| 21 CFR 820.20(c) | Cited across public-safe Form 483 observations | 1x |
| 21 CFR 820.30(i) | Cited across public-safe Form 483 observations | 1x |
Full site report
Get the verbatim findings behind Silq Technologies Corporation's 2 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