Home / Import refusals / 799-6397621-2/11/1

FDA Import Refusal 799-6397621-2/11/1 — Philips Ultrasound, LLC

Philips Ultrasound, LLC — FEI 3019216

The FDA refused shipment 799-6397621-2/11/1 from Philips Ultrasound, LLC (United States) on September 1, 2023. The refused product falls under Devices — SYSTEM, IMAGING, PULSED DOPPLER, ULTRASONIC. Cited charge: 118 This firm has 5 or more other import refusals on record.

Refusal Details

Date
September 1, 2023
Country
United States
Product Category
Devices
Product Code
90IYN SYSTEM, IMAGING, PULSED DOPPLER, ULTRASONIC
Charges
118

Recent inspections

  • 1253946 (OAI Fri Jan 31 2025 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1157069 (NAI Wed Nov 10 2021 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 761739 (VAI Fri Dec 09 2011 00:00:00 GMT+0000 (Coordinated Universal Time))

Other import refusals

  • 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)
  • 231-7498696-0/11/1 (Thu Mar 07 2019 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)

FDA data resources