FDA Import Refusal AEK-4603941-5/11/1 — Sonomed, Inc.
The FDA refused shipment AEK-4603941-5/11/1 from Sonomed, Inc. (United States) on Jul 13, 2018. The refused product falls under Devices — SYSTEM, IMAGING, PULSED ECHO, ULTRASONIC. Cited charge: 3280 This firm has 1 other import refusal on record.
Refusal Details
- Date
- Jul 13, 2018
- Country
- United States
- Product Category
- Devices
- Product Code
- 90IYO SYSTEM, IMAGING, PULSED ECHO, ULTRASONIC
- Charges
- 3280