Overview
- 8 public-safe observations are available for this inspection.
- 4 structured CFR citations are represented.
- 1 investigator is tied to this Form 483.
Inspectional observations
Each observation cites the regulation FDA found the firm out of compliance with.
20 May 2026
ISO 13485:2016 Clause 7.3.9
Records of design and development changes and their reviews not maintained
Cited by Javonica F Penn
20 May 2026
ISO 13485:2016 Clause 7.3.9
Records of design and development changes and their reviews not maintained
Cited by Javonica F Penn
20 May 2026
ISO 13485:2016 Clause 7.4.1
Records of supplier (re)evaluation, selection, and monitoring not maintained
Cited by Javonica F Penn
20 May 2026
ISO 13485:2016 Clause 7.4.1
Records of supplier (re)evaluation, selection, and monitoring not maintained
Cited by Javonica F Penn
20 May 2026
ISO 13485:2016 Clause 7.5.6
Procedures for validation of processes not documented
Cited by Javonica F Penn
Inspected site
KMKlarity Medical Products LLCHeath, United States
Inspection team
Cited regulations
CFR citations associated with this Form 483.
| Citation | What it covers | Cited |
|---|---|---|
| ISO 13485:2016 Clause 7.3.9 | Cited across public-safe Form 483 observations | 2x |
| ISO 13485:2016 Clause 7.4.1 | 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 8.3.4 | Cited across public-safe Form 483 observations | 2x |
Full 483 report
Get the verbatim text of all 8 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