Overview
- 6 FDA inspections are on record.
- 3 inspections produced a Form 483.
- The most recent recorded inspection date is 2026-04-01.
At a glance
Inspections
6
Form 483s
3
EIRs
0
Last outcome
Form 483
Inspection history
FDA inspections on record, most recent first.
| Inspection | Category | Outcome | Form 483 |
|---|---|---|---|
| 31 Mar 2026 – 1 Apr 2026 | Medical Devices & Rad Health | 483 | View 483 → |
| 7 Aug 2018 – 8 Aug 2018 | Medical Devices & Rad Health | 483 | View 483 → |
| 24 Oct 2013 | Medical Devices & Rad Health | 483 | View 483 → |
| 3 Nov 2010 | Not recorded | Clean | |
| 15 Jun 2007 | Not recorded | Clean | |
| 14 Feb 2002 | Not recorded | Clean |
Observations on record
Form 483 observations cited at this site, most recent first.
1 Apr 2026
ISO 13485:2016 Clause 8.2.2
Complaint handling procedures lack required elements
Cited by Clifford F Long
8 Aug 2018
21 CFR 820.30(g)
Design Validation - Risk analysis not performed/inadequate
Cited by Amanda Dinaro
8 Aug 2018
21 CFR 820.30(g)
Design Validation - Risk analysis not performed/inadequate
Cited by Amanda Dinaro
24 Oct 2013
21 CFR 820.30(g)
Design Validation - Risk analysis not performed/inadequate
Cited by Kimberly Lewandowski-Walker
Investigators
FDA investigators tied to this site in the record.
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 | 3x |
| ISO 13485:2016 Clause 8.2.2 | Cited across public-safe Form 483 observations | 1x |
Full site report
Get the verbatim findings behind M D Technologies, Inc.'s 3 Form 483s
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