FDA Import Refusal D51-1129944-7/3/1 — Philips North America, LLC

Philips North America, LLC — FEI 1218950

The FDA refused shipment D51-1129944-7/3/1 from Philips North America, LLC (United States) on Jan 8, 2014. The refused product falls under Devices — SYSTEM, IMAGING, PULSED DOPPLER, ULTRASONIC. Cited charges: 118,2480,341,508,84 This firm has 5 or more other import refusals on record.

Refusal Details

Date
Jan 8, 2014
Country
United States
Product Category
Devices
Product Code
90IYN SYSTEM, IMAGING, PULSED DOPPLER, ULTRASONIC
Charges
118,2480,341,508,84

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.