Overview
- 9 public-safe observations are available for this inspection.
- 2 structured CFR citations are represented.
- 2 investigators are tied to this Form 483.
Inspectional observations
Each observation cites the regulation FDA found the firm out of compliance with.
16 Dec 2015
21 CFR 820.30(f)
Design verification - output does not meet input requirement
Cited by Shafiq Ahadi, Karen M Montgomery
16 Dec 2015
21 CFR 820.30(f)
Design verification - output does not meet input requirement
Cited by Shafiq Ahadi, Karen M Montgomery
16 Dec 2015
21 CFR 820.30(f)
Design verification - output does not meet input requirement
Cited by Shafiq Ahadi, Karen M Montgomery
16 Dec 2015
21 CFR 820.30(g)
Design Validation - Risk analysis not performed/inadequate
Cited by Shafiq Ahadi, Karen M Montgomery
16 Dec 2015
21 CFR 820.30(g)
Design Validation - Risk analysis not performed/inadequate
Cited by Shafiq Ahadi, Karen M Montgomery
Inspected site
EIElekta IncSaint Charles, United States
Inspection team
Cited regulations
CFR citations associated with this Form 483.
| Citation | What it covers | Cited |
|---|---|---|
| 21 CFR 820.30(g) | Cited across public-safe Form 483 observations | 6x |
| 21 CFR 820.30(f) | Cited across public-safe Form 483 observations | 3x |
Full 483 report
Get the verbatim text of all 9 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