FDA Import Refusal AEK-1625100-8/1/1 — Principi De Piemon

Principi De Piemon — FEI 3011947412

The FDA refused shipment AEK-1625100-8/1/1 from Principi De Piemon (Italy) on Jan 7, 2016. The refused product falls under Devices — SYSTEM, OPTICAL IMPRESSION, COMPUTER ASSISTED DESIGN AND MANUFACTURING (CAD/CAM) OF DENTAL RESTORATI. Cited charge: 476

Refusal details

Date
Jan 7, 2016
Country
Italy
Product Category
Devices
Product Code
76NOF SYSTEM, OPTICAL IMPRESSION, COMPUTER ASSISTED DESIGN AND MANUFACTURING (CAD/CAM) OF DENTAL RESTORATI
Charges
476

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