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FDA Import Refusal 231-7498696-0/11/1 — Philips Ultrasound, LLC

Philips Ultrasound, LLC — FEI 3019216

The FDA refused shipment 231-7498696-0/11/1 from Philips Ultrasound, LLC (United States) on March 7, 2019. The refused product falls under Devices — SYSTEM, IMAGING, PULSED DOPPLER, ULTRASONIC. Cited charges: 118,3280,508 This firm has 5 or more other import refusals on record.

Refusal Details

Date
March 7, 2019
Country
United States
Product Category
Devices
Product Code
90IYN SYSTEM, IMAGING, PULSED DOPPLER, ULTRASONIC
Charges
118,3280,508

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Other import refusals

  • 799-6397621-2/11/1 (Fri Sep 01 2023 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • 799-6673609-0/11/1 (Fri Apr 17 2020 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • 799-4400082-5/11/1 (Wed Nov 27 2019 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • 799-0220768-5/11/1 (Tue Apr 02 2019 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • SCS-3580925-1/11/1 (Fri Mar 15 2019 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)

FDA data resources