FDA Import Refusal BOZ-0012250-3/2/1 — Drew Parc D'Activites

Drew Parc D'Activites — FEI 3008226477

The FDA refused shipment BOZ-0012250-3/2/1 from Drew Parc D'Activites (France) on Mar 20, 2017. The refused product falls under Devices — KIT, QUALITY CONTROL FOR BLOOD BANKING REAGENTS. Cited charge: 118

Refusal details

Date
Mar 20, 2017
Country
France
Product Category
Devices
Product Code
81KSF KIT, QUALITY CONTROL FOR BLOOD BANKING REAGENTS
Charges
118

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