FDA Import Refusal AEK-0495864-7/1/1 — Kj Meditech

Kj Meditech — FEI 3008253962

The FDA refused shipment AEK-0495864-7/1/1 from Kj Meditech (South Korea) on Aug 8, 2013. The refused product falls under Devices — IMPLANT, ENDOSSEOUS. Cited charge: 341 This firm has 3 other import refusals on record.

Refusal details

Date
Aug 8, 2013
Country
South Korea
Product Category
Devices
Product Code
76DZE IMPLANT, ENDOSSEOUS
Charges
341

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