FDA Import Refusal AEK-5835435-6/11/1 — Interojo Inc.

Interojo Inc. — FEI 3004146030

The FDA refused shipment AEK-5835435-6/11/1 from Interojo Inc. (South Korea) on Jan 29, 2025. The refused product falls under Devices — LENSES, SOFT CONTACT, DAILY WEAR. Cited charge: 2480 This firm has 5 or more other import refusals on record.

Refusal Details

Date
Jan 29, 2025
Country
South Korea
Product Category
Devices
Product Code
86LPL LENSES, SOFT CONTACT, DAILY WEAR
Charges
2480

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