FDA Import Refusal 799-8002996-9/11/1 — Lepu Medical Technology (Beijing) Co., Ltd.
The FDA refused shipment 799-8002996-9/11/1 from Lepu Medical Technology (Beijing) Co., Ltd. (China) on August 11, 2020. The refused product falls under Devices — SINGLE USE ONLY BLOOD LANCET WITH AN INTEGRAL SHARPS INJURY PREVENTION FEATURE. Cited charges: 118,341 This firm has 5 or more other import refusals on record.
Refusal Details
- Date
- August 11, 2020
- Country
- China
- Product Category
- Devices
- Product Code
- 79FMK SINGLE USE ONLY BLOOD LANCET WITH AN INTEGRAL SHARPS INJURY PREVENTION FEATURE
- Charges
- 118,341