FDA Inspection
Laboratory Corporation of America ViroMed LaboratoriesLaboratory Corporation of America ViroMed Laboratories – FDA Inspection, Aug 6, 2009
Record Details
This FDA Inspection record concerns Laboratory Corporation of America ViroMed Laboratories, with an inspection on August 6, 2009, issued by the Center for Biologics Evaluation and Research, covering biologics.
- Inspection Date
- August 6, 2009
- Product Type
- Biologics
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ID · 34542bbe-f875-4ef1-af3c-e05429c30df4
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 599070
- FDA center
- Biologics
- Project area
- Human Cellular, Tissue, and Gene Therapies
FDA Citations
1- 21 CFR 1271.47(a)Procedures for all other requirements
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Other FDA inspections of Laboratory Corporation of America ViroMed Laboratories
9| Date | Classification | Office | Project area |
|---|---|---|---|
| October 11, 2023 | NAI | Center for Biologics Evaluation and Research | Human Cellular, Tissue, and Gene Therapies |
| March 10, 2020 | NAI | Center for Biologics Evaluation and Research | Human Cellular, Tissue, and Gene Therapies |
| October 26, 2017 | NAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
| February 1, 2016 | NAI | Center for Biologics Evaluation and Research | Human Cellular, Tissue, and Gene Therapies |
| July 10, 2015 | NAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
Other documents for Laboratory Corporation of America ViroMed Laboratories
- FDA Inspection 1220851 - 2023-10-11
- FDA Inspection 1123198 - 2020-03-10
- FDA Inspection 1030800 - 2017-10-26
- FDA Inspection 958051 - 2016-02-01
- FDA Inspection 934670 - 2015-07-10
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