FDA Inspection
TriCore Reference LaboratoriesTriCore Reference Laboratories – FDA Inspection, Jul 19, 2013
Record Details
This FDA Inspection record concerns TriCore Reference Laboratories, with an inspection on July 19, 2013, issued by the Center for Biologics Evaluation and Research, covering biologics.
- Inspection Date
- July 19, 2013
- Product Type
- Biologics
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ID · cc7f6eb0-2e95-4624-aae9-617876b095c0
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 842499
- FDA center
- Biologics
- Project area
- Human Cellular, Tissue, and Gene Therapies
FDA Citations
1- 21 CFR 606.100(c)Thorough investigations
Full citation text and observation details available on the Dashboard.
Other FDA inspections of TriCore Reference Laboratories
4| Date | Classification | Office | Project area |
|---|---|---|---|
| March 21, 2017 | NAI | Center for Biologics Evaluation and Research | Human Cellular, Tissue, and Gene Therapies |
| February 11, 2015 | NAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
| December 8, 2011 | NAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
| December 21, 2009 | NAI | Center for Biologics Evaluation and Research | Human Cellular, Tissue, and Gene Therapies |
Other documents for TriCore Reference Laboratories
- FDA Inspection 1005189 - 2017-03-21
- FDA Inspection 913861 - 2015-02-11
- FDA Inspection 766941 - 2011-12-08
- FDA Inspection 635694 - 2009-12-21
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