Home / Import refusals / 799-0220768-5/11/1

FDA Import Refusal 799-0220768-5/11/1 — Philips Ultrasound, LLC

Philips Ultrasound, LLC — FEI 3019216

The FDA refused shipment 799-0220768-5/11/1 from Philips Ultrasound, LLC (United States) on April 2, 2019. The refused product falls under Devices — TRANSDUCER, ULTRASONIC, DIAGNOSTIC. Cited charges: 118,508 This firm has 5 or more other import refusals on record.

Refusal Details

Date
April 2, 2019
Country
United States
Product Category
Devices
Product Code
90ITX TRANSDUCER, ULTRASONIC, DIAGNOSTIC
Charges
118,508

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

  • 799-6397621-2/11/1 (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)
  • 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