FDA Import Refusal 799-9029596-4/12/1 — Shenzhen Imdk Medical Technology Co., Ltd.
The FDA refused shipment 799-9029596-4/12/1 from Shenzhen Imdk Medical Technology Co., Ltd. (China) on Oct 19, 2020. The refused product falls under Devices — NEBULIZER (DIRECT PATIENT INTERFACE). Cited charges: 118,3280,508 This firm has 5 or more other import refusals on record.
Refusal details
- Date
- Oct 19, 2020
- Country
- China
- Product Category
- Devices
- Product Code
- 73CAF NEBULIZER (DIRECT PATIENT INTERFACE)
- Charges
- 118,3280,508