Home / Import refusals / AEK-1331997-1/3/1D

FDA Import Refusal AEK-1331997-1/3/1D — Suzhou Armocon Technology Co.Ltd

Suzhou Armocon Technology Co.Ltd — FEI 3007962592

The FDA refused shipment AEK-1331997-1/3/1D from Suzhou Armocon Technology Co.Ltd (China) on May 7, 2014. The refused product falls under Devices — MASSAGER, THERAPEUTIC, ELECTRIC. Cited charge: 16 This firm has 5 or more other import refusals on record.

Refusal Details

Date
May 7, 2014
Country
China
Product Category
Devices
Product Code
89ISA MASSAGER, THERAPEUTIC, ELECTRIC
Charges
16

Recent inspections

  • 947350 (NAI Thu Sep 17 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 841203 (OAI Thu Jul 11 2013 00:00:00 GMT+0000 (Coordinated Universal Time))

Compliance actions

Other import refusals

  • 112-9633474-6/1/1 (Fri Mar 24 2017 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • AEK-1371986-5/4/1 (Fri May 23 2014 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • AEK-1373301-5/5/4 (Wed May 21 2014 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • AEK-1373301-5/5/2 (Wed May 21 2014 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • AEK-1373301-5/5/1 (Wed May 21 2014 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)

FDA data resources