FDA Import Refusal AEK-4365467-9/11/1 — Interojo Inc.

Interojo Inc. — FEI 3004146030

The FDA refused shipment AEK-4365467-9/11/1 from Interojo Inc. (South Korea) on Apr 5, 2018. The refused product falls under Devices — LENSES, SOFT CONTACT, DAILY WEAR. Cited charges: 118,3280,341,84 This firm has 5 or more other import refusals on record.

Refusal details

Date
Apr 5, 2018
Country
South Korea
Product Category
Devices
Product Code
86LPL LENSES, SOFT CONTACT, DAILY WEAR
Charges
118,3280,341,84

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