FDA Import Refusal AEK-0863913-7/3/1 — San Il Precision Industry

San Il Precision Industry — FEI 3011400578

The FDA refused shipment AEK-0863913-7/3/1 from San Il Precision Industry (South Korea) on Apr 8, 2015. The refused product falls under Devices — INSTRUMENT, MANUAL, GENERAL SURGICAL. Cited charges: 118,16,3280,333

Refusal details

Date
Apr 8, 2015
Country
South Korea
Product Category
Devices
Product Code
79MDM INSTRUMENT, MANUAL, GENERAL SURGICAL
Charges
118,16,3280,333

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