FDA Import Refusal AEK-2998275-5/11/1 — BEIJING GLOBALIPL DEVELOPMENT CO Ltd
The FDA refused shipment AEK-2998275-5/11/1 from BEIJING GLOBALIPL DEVELOPMENT CO Ltd (China) on Mar 6, 2017. The refused product falls under Devices — POWERED LASER SURGICAL INSTRUMENTS. Cited charges: 118,3280,508 This firm has 4 other import refusals on record.
Refusal details
- Date
- Mar 6, 2017
- Country
- China
- Product Category
- Devices
- Product Code
- 79GEX POWERED LASER SURGICAL INSTRUMENTS
- Charges
- 118,3280,508