FDA Inspection 897330 — Bioventus LLC

Bioventus LLC — FEI 3009595577

The FDA completed an inspection of Bioventus LLC on Jun 10, 2014 in Durham, NC. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Jun 10, 2014
Fiscal Year
2014
Product Type
Devices
Project Area
Compliance: Devices
Location
Durham, NC (United States)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.