Overview
- 2 FDA inspections are on record.
- 1 inspection produced a Form 483.
- The most recent recorded inspection date is 2026-05-06.
At a glance
Inspections
2
Form 483s
1
EIRs
0
Last outcome
Form 483
Inspection history
FDA inspections on record, most recent first.
| Inspection | Category | Outcome | Form 483 |
|---|---|---|---|
| 5 May 2026 – 6 May 2026 | Medical Devices & Rad Health | 483 | View 483 → |
| 7 Sep 2023 – 12 Sep 2023 | Medical Devices & Rad Health | Clean |
Observations on record
Form 483 observations cited at this site, most recent first.
6 May 2026
21 CFR 830.300(a)
Devices subject to device identification GUDID data submission requirements.
Cited by Eric C Schmitt
6 May 2026
21 CFR 830.300(a)
Devices subject to device identification GUDID data submission requirements.
Cited by Eric C Schmitt
Investigators
FDA investigators tied to this site in the record.
Eric C Schmitt2 insp.
Recurring citations
CFR citation patterns observed across this site's inspections.
| Citation | What it covers | Cited |
|---|---|---|
| 21 CFR 830.300(a) | Cited across public-safe Form 483 observations | 2x |
Full site report
Get the verbatim findings behind Pulsar Scientific LLC's 1 Form 483
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