Overview
- 2 public-safe observations are available for this inspection.
- 1 structured CFR citation is represented.
- 1 investigator is tied to this Form 483.
Inspectional observations
Each observation cites the regulation FDA found the firm out of compliance with.
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
Inspected site
PSPulsar Scientific LLCLudlow, United States
Inspection team
Cited regulations
CFR citations associated with this Form 483.
| Citation | What it covers | Cited |
|---|---|---|
| 21 CFR 830.300(a) | Cited across public-safe Form 483 observations | 2x |
Full 483 report
Get the verbatim text of all 2 observations
The full inspection record, as Atlas holds it, so your team sees exactly what was cited and how it was answered.
- The site's full inspection history around this Form 483
- Whether these citations escalated to a warning letter
- The investigators involved and the citations they repeat elsewhere