Overview
- 2 FDA inspections are on record.
- 2 inspections produced a Form 483.
- The most recent recorded inspection date is 2026-01-09.
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 |
|---|---|---|---|
| 5 Jan 2026 – 9 Jan 2026 | Medical Devices & Rad Health | 483 | View 483 → |
| 10 Apr 2017 – 13 Apr 2017 | Medical Devices & Rad Health | 483 | On file |
Observations on record
Form 483 observations cited at this site, most recent first.
9 Jan 2026
21 CFR 820.70(b)
Production and Process Change Procedures, lack of or Inad.
Cited by Joshua J Silvestri
Investigators
FDA investigators tied to this site in the record.
Joshua J Silvestri1 insp.
Sarah A Hassas1 insp.
Recurring citations
CFR citation patterns observed across this site's inspections.
| Citation | What it covers | Cited |
|---|---|---|
| 21 CFR 820.70(b) | Cited across public-safe Form 483 observations | 1x |
| 21 CFR 820.70(g)(3) | Cited across public-safe Form 483 observations | 1x |
Full site report
Get the verbatim findings behind HG Medical Gmbh's 2 Form 483s
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