Overview
- 5 public-safe observations are available for this inspection.
- 5 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.
30 Sep 2009
21 CFR 606.65(c)
Testing of representative samples of reagent lots
Cited by Kimberly Y Martin
30 Sep 2009
21 CFR 606.100(b)
Establish, maintain and follow manufacturing SOPs
Cited by Kimberly Y Martin
30 Sep 2009
21 CFR 606.100(b)(12)
Criteria for suitability of reissue of returned blood
Cited by Kimberly Y Martin
Inspected site
QDQuest DiagnosticsIndianapolis, United States
Inspection team
Cited regulations
CFR citations associated with this Form 483.
| Citation | What it covers | Cited |
|---|---|---|
| 21 CFR 606.100(b) | Cited across public-safe Form 483 observations | 1x |
| 21 CFR 606.100(b)(12) | Cited across public-safe Form 483 observations | 1x |
| 21 CFR 606.171 | Cited across public-safe Form 483 observations | 1x |
| 21 CFR 606.20(b) | Cited across public-safe Form 483 observations | 1x |
| 21 CFR 606.65(c) | 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