FDA Import Refusal AEK-8618079-7/1/1 — Teratech Corporation
The FDA refused shipment AEK-8618079-7/1/1 from Teratech Corporation (United States) on Nov 7, 2011. The refused product falls under Devices — SYSTEM, IMAGING, PULSED DOPPLER, ULTRASONIC. Cited charge: 341
Refusal Details
- Date
- Nov 7, 2011
- Country
- United States
- Product Category
- Devices
- Product Code
- 90IYN SYSTEM, IMAGING, PULSED DOPPLER, ULTRASONIC
- Charges
- 341