FDA Import Refusal AEK-7983127-4/11/1 — SHANDONG HUAMEI TECHNOLOGY CO.,LTD.
The FDA refused shipment AEK-7983127-4/11/1 from SHANDONG HUAMEI TECHNOLOGY CO.,LTD. (China) on Nov 12, 2020. The refused product falls under Devices — POWERED LASER SURGICAL INSTRUMENTS. Cited charge: 476 This firm has 5 or more other import refusals on record.
Refusal Details
- Date
- Nov 12, 2020
- Country
- China
- Product Category
- Devices
- Product Code
- 79GEX POWERED LASER SURGICAL INSTRUMENTS
- Charges
- 476