# FDA Inspection 897330 - Bioventus LLC - June 10, 2014

Source: https://www.keypedia.com/records/fda_inspections/bioventus-llc/67d6c12a-e75e-40bb-bbb5-4ff90f40ed7d
Source feed: FDA_Inspections

> FDA Inspection 897330 for Bioventus LLC on June 10, 2014. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 897330
- Company Name: Bioventus LLC
- Inspection Date: 2014-06-10
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 897330 - 2014-06-10](https://www.keypedia.com/records/fda_inspections/bioventus-llc/2ef3b81d-5d2e-42ee-a2fd-c2e9125c4077)

Company: https://www.keypedia.com/companies/bioventus-llc/56863798-0f7f-4435-a216-d518220cbc18

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