Home / Import refusals / AEK-2310202-0/1/1

FDA Import Refusal AEK-2310202-0/1/1 — Solta Medical Inc

Solta Medical Inc — FEI 3003079710

The FDA refused shipment AEK-2310202-0/1/1 from Solta Medical Inc (United States) on August 12, 2016. The refused product falls under Devices — KIT, SURGICAL INSTRUMENT, DISPOSABLE. Cited charges: 118,3280,341 This firm has 4 other import refusals on record.

Refusal Details

Date
August 12, 2016
Country
United States
Product Category
Devices
Product Code
79KDD KIT, SURGICAL INSTRUMENT, DISPOSABLE
Charges
118,3280,341

Recent inspections

  • 882308 (VAI Tue Jun 17 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 873862 (NAI Thu Apr 10 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 798415 (OAI Fri Aug 17 2012 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 755598 (NAI Fri Dec 02 2011 00:00:00 GMT+0000 (Coordinated Universal Time))

Compliance actions

Other import refusals

  • ES3-2528351-4/51/1 (Fri Aug 31 2018 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • DO7-7810269-2/1/1 (Fri Nov 06 2015 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • ANQ-2030199-0/1/1 (Tue Aug 18 2015 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • 9TV-0000378-0/1/1 (Wed Feb 25 2015 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)

FDA data resources