Overview
- 5 public-safe observations are available for this inspection.
- 5 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.
20 Nov 2008
21 CFR 1271.47(a)
Procedures for all other requirements
Cited by Catherine V Quinlan, Gary D Urbiel Goldner
20 Nov 2008
21 CFR 1271.47(e)
Adopting procedures from another organization
Cited by Catherine V Quinlan, Gary D Urbiel Goldner
20 Nov 2008
21 CFR 1271.55(a)(2)
Eligibility statement--basis of determination
Cited by Catherine V Quinlan, Gary D Urbiel Goldner
20 Nov 2008
21 CFR 1271.55(a)(3)
Summary--records used to make determination
Cited by Catherine V Quinlan, Gary D Urbiel Goldner
20 Nov 2008
21 CFR 1271.80(b)
Specimen collections not timely
Cited by Catherine V Quinlan, Gary D Urbiel Goldner
Inspected site
HFHenry Ford Center for Reproductive MedicineTroy, United States
Inspection team
Cited regulations
CFR citations associated with this Form 483.
| Citation | What it covers | Cited |
|---|---|---|
| 21 CFR 1271.47(a) | Cited across public-safe Form 483 observations | 1x |
| 21 CFR 1271.47(e) | Cited across public-safe Form 483 observations | 1x |
| 21 CFR 1271.55(a)(2) | Cited across public-safe Form 483 observations | 1x |
| 21 CFR 1271.55(a)(3) | Cited across public-safe Form 483 observations | 1x |
| 21 CFR 1271.80(b) | Cited across public-safe Form 483 observations | 1x |
Full 483 report
Get the verbatim text of all 5 observations
Every observation in full, 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