Overview
- 6 public-safe observations are available for this inspection.
- 6 structured CFR citations are represented.
- 3 investigators are tied to this Form 483.
Inspectional observations
Each observation cites the regulation FDA found the firm out of compliance with.
19 Apr 2024
21 CFR 600.14(a)(1)
Who must report - manufacturer
Cited by Richard T Riggie, Creighton T Tuzon, Elias N Paz Alonzo
19 Apr 2024
21 CFR 803.17(b)(1)
Info evaluated to determine if event was reportable
Cited by Richard T Riggie, Creighton T Tuzon, Elias N Paz Alonzo
19 Apr 2024
21 CFR 803.50(a)(2)
Individual Report of Malfunction
Cited by Richard T Riggie, Creighton T Tuzon, Elias N Paz Alonzo
19 Apr 2024
21 CFR 820.150
Lack of or inadequate procedures for storage.
Cited by Richard T Riggie, Creighton T Tuzon, Elias N Paz Alonzo
19 Apr 2024
21 CFR 820.30(g)
Design Validation - Risk analysis not performed/inadequate
Cited by Richard T Riggie, Creighton T Tuzon, Elias N Paz Alonzo
Inspected site
DDIAGASTLoos, France
Inspection team
Cited regulations
CFR citations associated with this Form 483.
| Citation | What it covers | Cited |
|---|---|---|
| 21 CFR 600.14(a)(1) | Cited across public-safe Form 483 observations | 1x |
| 21 CFR 803.17(b)(1) | Cited across public-safe Form 483 observations | 1x |
| 21 CFR 803.50(a)(2) | Cited across public-safe Form 483 observations | 1x |
| 21 CFR 820.150 | Cited across public-safe Form 483 observations | 1x |
| 21 CFR 820.30(g) | Cited across public-safe Form 483 observations | 1x |
| 21 CFR 820.80(c) | Cited across public-safe Form 483 observations | 1x |
Source document
PDF
PDF available
Form 483 source document
The source document is available to authorized Atlas users.
Full 483 report
Get the verbatim text of all 6 observations
The source PDF, 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