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FDA Import Refusal 799-7705798-3/11/1 — Kinamed Inc

Kinamed Inc — FEI 2027148

The FDA refused shipment 799-7705798-3/11/1 from Kinamed Inc (United States) on November 17, 2023. The refused product falls under Devices — ORTHOPEDIC MANUAL SURGICAL INSTRUMENT. Cited charges: 118,3280,508

Refusal Details

Date
November 17, 2023
Country
United States
Product Category
Devices
Product Code
87LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT
Charges
118,3280,508

Recent inspections

  • 1117751 (NAI Wed Feb 12 2020 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 980471 (NAI Thu Jul 21 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 875744 (NAI Mon Apr 14 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 773213 (NAI Thu Mar 15 2012 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 663654 (VAI Tue Jun 01 2010 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources