FDA Inspection
Quest DiagnosticsQuest Diagnostics – FDA Inspection, Sep 22, 2010
Record Details
This FDA Inspection record concerns Quest Diagnostics, with an inspection on September 22, 2010, issued by the Center for Biologics Evaluation and Research, covering biologics.
- Company
- Quest Diagnostics
- Inspection Date
- September 22, 2010
- Product Type
- Biologics
View Company Profile
ID · 19814b2a-c984-4339-b14f-0e2f617ce1f4
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 681842
- FDA center
- Biologics
- Project area
- Blood and Blood Products
FDA Citations
1- 21 CFR 600.10(b)Personnel capabilities
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Quest Diagnostics
6| Date | Classification | Office | Project area |
|---|---|---|---|
| July 30, 2024 | NAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
| September 13, 2018 | NAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
| August 25, 2016 | VAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
| July 28, 2014 | VAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
| September 18, 2012 | VAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
Other documents for Quest Diagnostics
- FDA Inspection 1245312 - 2024-07-30
- FDA Inspection 1069321 - 2018-09-13
- FDA Inspection 983437 - 2016-08-25
- FDA Inspection 889102 - 2014-07-28
- FDA Inspection 799707 - 2012-09-18
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