FDA Import Refusal AEK-1535601-4/1/1 — Bioventus LLC

Bioventus LLC — FEI 3009595577

The FDA refused shipment AEK-1535601-4/1/1 from Bioventus LLC (United States) on Dec 3, 2015. The refused product falls under Devices — STIMULATOR, BONE GROWTH, NON-INVASIVE. Cited charges: 118,16,341 This firm has 2 other import refusals on record.

Refusal Details

Date
Dec 3, 2015
Country
United States
Product Category
Devices
Product Code
89LOF STIMULATOR, BONE GROWTH, NON-INVASIVE
Charges
118,16,341

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