FDA Import Refusal 310-5109931-0/1/1 — Verathon, Inc.
The FDA refused shipment 310-5109931-0/1/1 from Verathon, Inc. (United States) on Feb 17, 2002. The refused product falls under Devices — SYSTEM, IMAGING, PULSED ECHO, ULTRASONIC. Cited charge: 118 This firm has 2 other import refusals on record.
Refusal Details
- Date
- Feb 17, 2002
- Country
- United States
- Product Category
- Devices
- Product Code
- 90IYO SYSTEM, IMAGING, PULSED ECHO, ULTRASONIC
- Charges
- 118