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FDA Import Refusal AEK-1373301-5/5/2 — Suzhou Armocon Technology Co.Ltd

Suzhou Armocon Technology Co.Ltd — FEI 3007962592

The FDA refused shipment AEK-1373301-5/5/2 from Suzhou Armocon Technology Co.Ltd (China) on May 21, 2014. The refused product falls under Devices — DEVICE, EXTERNAL PENILE RIGIDITY. Cited charge: 237 This firm has 5 or more other import refusals on record.

Refusal Details

Date
May 21, 2014
Country
China
Product Category
Devices
Product Code
78LKY DEVICE, EXTERNAL PENILE RIGIDITY
Charges
237

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-1373301-5/5/1 (Wed May 21 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-1331997-1/3/1A (Wed May 07 2014 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)

FDA data resources