Home / Import refusals / AEK-5047811-1/11/1

FDA Import Refusal AEK-5047811-1/11/1 — Zimmer, Inc.

Zimmer, Inc. — FEI 1000220733

The FDA refused shipment AEK-5047811-1/11/1 from Zimmer, Inc. (United States) on October 23, 2018. The refused product falls under Devices — ARTHROSCOPE AND ACCESSORIES. Cited charges: 118,3280 This firm has 5 or more other import refusals on record.

Refusal Details

Date
October 23, 2018
Country
United States
Product Category
Devices
Product Code
87HRX ARTHROSCOPE AND ACCESSORIES
Charges
118,3280

Recent inspections

  • 1177397 (NAI Wed Jul 27 2022 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1029453 (VAI Mon Oct 16 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 951676 (OAI Fri Nov 20 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 880647 (OAI Wed May 28 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 865719 (VAI Fri Feb 07 2014 00:00:00 GMT+0000 (Coordinated Universal Time))

Other import refusals

  • 799-5029690-0/1/1 (Wed Apr 20 2016 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • BIP-0022317-4/1/1 (Fri Oct 30 2015 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • 799-0508998-8/1/35 (Tue Jun 23 2015 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • 799-0508998-8/1/37 (Tue Jun 23 2015 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • 799-0508998-8/1/2 (Tue Jun 23 2015 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)

FDA data resources