Home / Import refusals / AEK-2887253-6/21/1

FDA Import Refusal AEK-2887253-6/21/1 — Zhejiang Biomet Medical Products Co. Ltd.

Zhejiang Biomet Medical Products Co. Ltd. — FEI 3006801265

The FDA refused shipment AEK-2887253-6/21/1 from Zhejiang Biomet Medical Products Co. Ltd. (China) on November 21, 2017. The refused product falls under Devices — REAMER. Cited charge: 118 This firm has 5 or more other import refusals on record.

Refusal Details

Date
November 21, 2017
Country
China
Product Category
Devices
Product Code
87HTO REAMER
Charges
118

Recent inspections

  • 1026172 (NAI Thu Aug 17 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 913071 (NAI Thu Jan 22 2015 00:00:00 GMT+0000 (Coordinated Universal Time))

Compliance actions

Other import refusals

  • AEK-2879020-9/11/1 (Tue Nov 21 2017 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • AEK-2887253-6/41/1 (Tue Nov 21 2017 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • AEK-2887253-6/31/1 (Tue Nov 21 2017 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • AEK-2879020-9/21/1 (Tue Nov 21 2017 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • AEK-2887253-6/11/1 (Tue Nov 21 2017 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)

FDA data resources