FDA Import Refusal AEK-9464200-3/12/1 — SHANDONG HUAMEI TECHNOLOGY CO.,LTD.
The FDA refused shipment AEK-9464200-3/12/1 from SHANDONG HUAMEI TECHNOLOGY CO.,LTD. (China) on Aug 4, 2021. The refused product falls under Devices — POWERED LASER SURGICAL INSTRUMENTS. Cited charge: 47 This firm has 5 or more other import refusals on record.
Refusal Details
- Date
- Aug 4, 2021
- Country
- China
- Product Category
- Devices
- Product Code
- 79GEX POWERED LASER SURGICAL INSTRUMENTS
- Charges
- 47