FDA Inspection
Osteotech, Inc.Osteotech, Inc. – FDA Inspection, Jul 30, 2018
Record Details
This FDA Inspection record concerns Osteotech, Inc., with an inspection on July 30, 2018, issued by the Center for Biologics Evaluation and Research, covering biologics.
View Company Profile
ID · 53653e50-b1c2-439f-9985-fa3c1388351b
Inspection Facts
No Action Indicated (NAI)
No objectionable conditions or practices were found during the inspection.
- Inspection number
- 1060874
- FDA center
- Biologics
- Project area
- Human Cellular, Tissue, and Gene Therapies
Other FDA inspections of Osteotech, Inc.
8| Date | Classification | Office | Project area |
|---|---|---|---|
| June 18, 2024 | NAI | Center for Biologics Evaluation and Research | Human Cellular, Tissue, and Gene Therapies |
| August 12, 2021 | NAI | Center for Biologics Evaluation and Research | Human Cellular, Tissue, and Gene Therapies |
| August 10, 2017 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| May 6, 2015 | NAI | Center for Biologics Evaluation and Research | Human Cellular, Tissue, and Gene Therapies |
| August 16, 2013 | NAI | Center for Biologics Evaluation and Research | Human Cellular, Tissue, and Gene Therapies |
Other documents for Osteotech, Inc.
- FDA Inspection 1245789 - 2024-06-18
- FDA Inspection 1150237 - 2021-08-12
- FDA Inspection 1021037 - 2017-08-10
- FDA Inspection 925160 - 2015-05-06
- FDA Inspection 845708 - 2013-08-16
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