FDA Import Refusal AEK-6314394-2/11/1 — Zhejiang Supor Pharmaceuticals Co., Ltd.
The FDA refused shipment AEK-6314394-2/11/1 from Zhejiang Supor Pharmaceuticals Co., Ltd. (China) on September 18, 2019. The refused product falls under Drugs and Biologics — KETOTIFEN FUMERATE (ANTI-ASTHMATIC). Cited charge: 16 This firm has 1 other import refusal on record.
Refusal Details
- Date
- September 18, 2019
- Country
- China
- Product Category
- Drugs and Biologics
- Product Code
- 61ECR14 KETOTIFEN FUMERATE (ANTI-ASTHMATIC)
- Charges
- 16