FDA Import Refusal AEK-5412242-6/11/1 — BEIJING KAI DI TAI MEDICAL TECHN

BEIJING KAI DI TAI MEDICAL TECHN — FEI 3014914389

The FDA refused shipment AEK-5412242-6/11/1 from BEIJING KAI DI TAI MEDICAL TECHN (China) on Dec 13, 2018. The refused product falls under Devices — IMPLANT, DERMAL, COLLAGEN FOR AESTHETIC USE. Cited charges: 118,237,3280,333

Refusal details

Date
Dec 13, 2018
Country
China
Product Category
Devices
Product Code
79LMH IMPLANT, DERMAL, COLLAGEN FOR AESTHETIC USE
Charges
118,237,3280,333

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