Overview
- 1 FDA inspection is on record.
- 1 inspection produced a Form 483.
- The most recent recorded inspection date is 2026-04-28.
At a glance
Inspections
1
Form 483s
1
EIRs
0
Last outcome
Form 483
Inspection history
FDA inspections on record, most recent first.
| Inspection | Category | Outcome | Form 483 |
|---|---|---|---|
| 23 Apr 2026 – 28 Apr 2026 | Medical Devices & Rad Health | 483 | View 483 → |
Observations on record
Form 483 observations cited at this site, most recent first.
28 Apr 2026
ISO 13485:2016 Clause 7.1
Records of risk management activities in product realization not maintained
Cited by James P Finn
28 Apr 2026
ISO 13485:2016 Clause 7.1
Records of risk management activities in product realization not maintained
Cited by James P Finn
28 Apr 2026
ISO 13485:2016 Clause 7.5.6
Procedures for validation of processes not documented
Cited by James P Finn
28 Apr 2026
ISO 13485:2016 Clause 7.5.6
Procedures for validation of processes not documented
Cited by James P Finn
28 Apr 2026
ISO 13485:2016 Clause 8.5.2
Corrective action procedures not documented
Cited by James P Finn
Investigators
FDA investigators tied to this site in the record.
James P Finn1 insp.
Recurring citations
CFR citation patterns observed across this site's inspections.
| Citation | What it covers | Cited |
|---|---|---|
| ISO 13485:2016 Clause 7.1 | Cited across public-safe Form 483 observations | 2x |
| ISO 13485:2016 Clause 7.5.6 | Cited across public-safe Form 483 observations | 2x |
| ISO 13485:2016 Clause 8.5.2 | Cited across public-safe Form 483 observations | 2x |
Full site report
Get the verbatim findings behind APMTD, INC.'s 1 Form 483
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