FDA Import Refusal AEK-0878796-0/12/1 — Medytox Inc.

Medytox Inc. — FEI 3014451374

The FDA refused shipment AEK-0878796-0/12/1 from Medytox Inc. (South Korea) on Apr 7, 2022. The refused product falls under Devices — IMPLANT, DERMAL, COLLAGEN FOR AESTHETIC USE. Cited charges: 118,237,2480,3280 This firm has 5 or more other import refusals on record.

Refusal details

Date
Apr 7, 2022
Country
South Korea
Product Category
Devices
Product Code
79LMH IMPLANT, DERMAL, COLLAGEN FOR AESTHETIC USE
Charges
118,237,2480,3280

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