FDA Inspection
CorneaGen - RichmondCorneaGen - Richmond – FDA Inspection, May 31, 2018
Record Details
This FDA Inspection record concerns CorneaGen - Richmond, with an inspection on May 31, 2018, issued by the Center for Biologics Evaluation and Research, covering biologics.
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ID · 78247ae5-77b6-4edd-a022-6a5d0698bed5
Inspection Facts
No Action Indicated (NAI)
No objectionable conditions or practices were found during the inspection.
- Inspection number
- 1059878
- FDA center
- Biologics
- Project area
- Blood and Blood Products
Other FDA inspections of CorneaGen - Richmond
3| Date | Classification | Office | Project area |
|---|---|---|---|
| May 12, 2016 | NAI | Center for Biologics Evaluation and Research | Human Cellular, Tissue, and Gene Therapies |
| February 12, 2013 | NAI | Center for Biologics Evaluation and Research | Human Cellular, Tissue, and Gene Therapies |
| June 13, 2011 | VAI | Center for Biologics Evaluation and Research | Human Cellular, Tissue, and Gene Therapies |
Other documents for CorneaGen - Richmond
- FDA Inspection 974353 - 2016-05-12
- FDA Inspection 823345 - 2013-02-12
- FDA Inspection 729194 - 2011-06-13
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