FDA Inspection 869241 — BIOVENTUS LLC

BIOVENTUS LLC — FEI 3027669735

The FDA completed an inspection of BIOVENTUS LLC on Mar 6, 2014 in Cordova, TN. 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
Mar 6, 2014
Fiscal Year
2014
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Cordova, TN (United States)

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