Home / Import refusals / AEK-1253912-4/1/1

FDA Import Refusal AEK-1253912-4/1/1 — Beijing Toplaser Technology Co., Ltd.

Beijing Toplaser Technology Co., Ltd. — FEI 3005450614

The FDA refused shipment AEK-1253912-4/1/1 from Beijing Toplaser Technology Co., Ltd. (China) on April 30, 2014. The refused product falls under Devices — POWERED LASER SURGICAL INSTRUMENTS. Cited charges: 118,16,2480,278,333,84 This firm has 5 or more other import refusals on record.

Refusal Details

Date
April 30, 2014
Country
China
Product Category
Devices
Product Code
79GEX POWERED LASER SURGICAL INSTRUMENTS
Charges
118,16,2480,278,333,84

Recent inspections

  • 926274 (OAI Thu Apr 02 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 756492 (VAI Thu Dec 01 2011 00:00:00 GMT+0000 (Coordinated Universal Time))

Other import refusals

  • AEK-3150851-5/11/1 (Wed Apr 19 2017 00:00:00 GMT+0000 (Coordinated Universal Time) — Radiological Health)
  • AEK-1462898-2/1/1 (Tue Jun 17 2014 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • UPS-6949816-6/1/1 (Wed Jul 25 2012 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • UPS-6949766-3/1/1 (Fri Jul 20 2012 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • 112-2705924-8/1/1 (Tue Jul 26 2011 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)

FDA data resources