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FDA Import Refusal 799-0723691-1/11/1 — Arrotek Medical Ltd

Arrotek Medical Ltd — FEI 3005255160

The FDA refused shipment 799-0723691-1/11/1 from Arrotek Medical Ltd (Ireland) on April 12, 2019. The refused product falls under Devices — SYSTEM, HYPERTHERMIA, RF/MICROWAVE (BENIGN PROSTATIC HYPERPLASIA). Cited charges: 118,508

Refusal Details

Date
April 12, 2019
Country
Ireland
Product Category
Devices
Product Code
78MEQ SYSTEM, HYPERTHERMIA, RF/MICROWAVE (BENIGN PROSTATIC HYPERPLASIA)
Charges
118,508

Recent inspections

  • 1203431 (NAI Tue Mar 07 2023 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 940228 (NAI Thu Jul 30 2015 00:00:00 GMT+0000 (Coordinated Universal Time))

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