FDA Import Refusal AEK-6113624-5/11/1 — Sonablate Corp.

Sonablate Corp. — FEI 3007126306

The FDA refused shipment AEK-6113624-5/11/1 from Sonablate Corp. (United States) on Jul 23, 2019. The refused product falls under Devices — SYSTEM, ABLATION, ULTRASOUND AND ACCESSORIES. Cited charges: 118,3280,508

Refusal Details

Date
Jul 23, 2019
Country
United States
Product Category
Devices
Product Code
79NTB SYSTEM, ABLATION, ULTRASOUND AND ACCESSORIES
Charges
118,3280,508