FDA Import Refusal AEK-5080125-4/11/1 — Philips Ultrasound, LLC
The FDA refused shipment AEK-5080125-4/11/1 from Philips Ultrasound, LLC (United States) on October 23, 2018. The refused product falls under Devices — TRANSDUCER, ULTRASONIC, DIAGNOSTIC. Cited charge: 3280 This firm has 5 or more other import refusals on record.
Refusal Details
- Date
- October 23, 2018
- Country
- United States
- Product Category
- Devices
- Product Code
- 90ITX TRANSDUCER, ULTRASONIC, DIAGNOSTIC
- Charges
- 3280