# FDA Inspection 919526 - NovaBone Products LLC - March 20, 2015

Source: https://www.keypedia.com/records/fda_inspections/novabone-products-llc/f32d06fe-76e8-4c6c-990f-5b555371dd2b
Source feed: FDA_Inspections

> FDA Inspection 919526 for NovaBone Products LLC on March 20, 2015. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 919526
- Company Name: NovaBone Products LLC
- Inspection Date: 2015-03-20
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 919526 - 2015-03-20](https://www.keypedia.com/records/fda_inspections/novabone-products-llc/e5164abc-4dc1-40e3-8f89-e4a072f41c60)
- [FDA Inspection 752755 - 2011-11-03](https://www.keypedia.com/records/fda_inspections/novabone-products-llc/8865d7e8-e314-493a-9f67-3e971a773dce)
- [FDA Inspection 752755 - 2011-11-03](https://www.keypedia.com/records/fda_inspections/novabone-products-llc/7f38ef68-018c-4452-bfcc-55acec6742b5)

Company: https://www.keypedia.com/companies/novabone-products-llc/5923b259-7787-4dfc-88fd-5cb39f8d3ba9

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7