FDA Import Refusal AEK-5032468-7/11/1 — Yumen Qianhua Pharmaceutical Co., Ltd.

Yumen Qianhua Pharmaceutical Co., Ltd. — FEI 3030638441

The FDA refused shipment AEK-5032468-7/11/1 from Yumen Qianhua Pharmaceutical Co., Ltd. (China) on Jul 24, 2018. The refused product falls under Drugs and Biologics — MINOXIDIL (ANTI-HYPERTENSIVE). Cited charges: 118,3280,75 This firm has 3 other import refusals on record.

Refusal details

Date
Jul 24, 2018
Country
China
Product Category
Drugs and Biologics
Product Code
62CDL41 MINOXIDIL (ANTI-HYPERTENSIVE)
Charges
118,3280,75

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