Home / Import refusals / HJ7-5009247-0/1/1

FDA Import Refusal HJ7-5009247-0/1/1 — Leica Biosystems Melbourne Pty Ltd

Leica Biosystems Melbourne Pty Ltd — FEI 3006461677

The FDA refused shipment HJ7-5009247-0/1/1 from Leica Biosystems Melbourne Pty Ltd (Australia) on October 26, 2016. The refused product falls under Devices — INSTRUMENTATION FOR CLINICAL MULIPLEX TEST SYSTEMS. Cited charge: 118 This firm has 5 or more other import refusals on record.

Refusal Details

Date
October 26, 2016
Country
Australia
Product Category
Devices
Product Code
75NSU INSTRUMENTATION FOR CLINICAL MULIPLEX TEST SYSTEMS
Charges
118

Recent inspections

  • 1012579 (NAI Thu May 11 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 809369 (NAI Thu Nov 22 2012 00:00:00 GMT+0000 (Coordinated Universal Time))

Other import refusals

  • 799-9398952-8/1/1 (Fri Mar 24 2017 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • HJ7-5009194-4/1/1 (Wed Oct 26 2016 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • HJ7-5009215-7/1/1 (Wed Oct 26 2016 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • 799-9363454-6/1/1 (Wed Jun 03 2015 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • 799-9363454-6/1/2 (Wed Jun 03 2015 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)

FDA data resources