FDA Inspection
Osteotech, Inc.Osteotech, Inc. – FDA Inspection, Aug 16, 2013
Record Details
This FDA Inspection record concerns Osteotech, Inc., with an inspection on August 16, 2013, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Osteotech, Inc.
- Inspection Date
- August 16, 2013
- Product Type
- Devices
View Company Profile
ID · 7f0db1ef-b91e-4473-b0a5-2bff6aaaaf6e
Inspection Facts
No Action Indicated (NAI)
No objectionable conditions or practices were found during the inspection.
- Inspection number
- 845698
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
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 |
| July 30, 2018 | 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 |
Other documents for Osteotech, Inc.
- FDA Inspection 1245789 - 2024-06-18
- FDA Inspection 1150237 - 2021-08-12
- FDA Inspection 1060874 - 2018-07-30
- FDA Inspection 1021037 - 2017-08-10
- FDA Inspection 925160 - 2015-05-06
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