# FDA Inspection 869241 - Bioventus, LLC - March 06, 2014

Source: https://www.globalkeysolutions.net/records/fda_inspections/bioventus-llc/15780de1-bbfb-4b25-a724-0219f23461c4
Source feed: FDA_Inspections

> FDA Inspection 869241 for Bioventus, LLC on March 06, 2014. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 869241
- Company Name: Bioventus, LLC
- Inspection Date: 2014-03-06
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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- [FDA Inspection 925979 - 2015-05-13](https://www.globalkeysolutions.net/records/fda_inspections/bioventus-llc/ddf49782-2125-48c7-83c2-09aa4d87c3dc)
- [FDA Inspection 869241 - 2014-03-06](https://www.globalkeysolutions.net/records/fda_inspections/bioventus-llc/443cdd22-f05f-4313-91b3-1648273aea9d)

Company: https://www.globalkeysolutions.net/companies/bioventus-llc/453be53a-0c51-419b-be91-c76e6a490b99

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