FDA Inspection
ReproTech, Ltd.ReproTech, Ltd. – FDA Inspection, Dec 15, 2015
Record Details
This FDA Inspection record concerns ReproTech, Ltd., with an inspection on December 15, 2015, issued by the Center for Biologics Evaluation and Research, covering biologics.
- Company
- ReproTech, Ltd.
- Inspection Date
- December 15, 2015
- Product Type
- Biologics
View Company Profile
ID · 793908df-4601-4cf8-adb1-57e361d5a729
Inspection Facts
No Action Indicated (NAI)
No objectionable conditions or practices were found during the inspection.
- Inspection number
- 952457
- FDA center
- Biologics
- Project area
- Human Cellular, Tissue, and Gene Therapies
Other FDA inspections of ReproTech, Ltd.
5| Date | Classification | Office | Project area |
|---|---|---|---|
| January 23, 2020 | NAI | Center for Biologics Evaluation and Research | Human Cellular, Tissue, and Gene Therapies |
| January 4, 2018 | NAI | Center for Biologics Evaluation and Research | Human Cellular, Tissue, and Gene Therapies |
| January 29, 2014 | NAI | Center for Biologics Evaluation and Research | Human Cellular, Tissue, and Gene Therapies |
| February 8, 2012 | NAI | Center for Biologics Evaluation and Research | Human Cellular, Tissue, and Gene Therapies |
| January 8, 2010 | NAI | Center for Biologics Evaluation and Research | Human Cellular, Tissue, and Gene Therapies |
Other documents for ReproTech, Ltd.
- FDA Inspection 1116523 - 2020-01-23
- FDA Inspection 1037727 - 2018-01-04
- FDA Inspection 863862 - 2014-01-29
- FDA Inspection 767137 - 2012-02-08
- FDA Inspection 637647 - 2010-01-08
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