FDA Import Refusal 336-7475237-8/21/1 — GRI Medical & Electronic Technology Co., Ltd.
The FDA refused shipment 336-7475237-8/21/1 from GRI Medical & Electronic Technology Co., Ltd. (China) on May 17, 2022. 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
- May 17, 2022
- Country
- China
- Product Category
- Devices
- Product Code
- 79FMK SINGLE USE ONLY BLOOD LANCET WITH AN INTEGRAL SHARPS INJURY PREVENTION FEATURE
- Charges
- 118,341