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FDA Import Refusal 799-2875296-3/11/1 — Plexus Corporation

Plexus Corporation — FEI 3004105270

The FDA refused shipment 799-2875296-3/11/1 from Plexus Corporation (United States) on March 24, 2023. The refused product falls under Devices — DEVICE, ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES. Cited charges: 3280,341

Refusal Details

Date
March 24, 2023
Country
United States
Product Category
Devices
Product Code
79GEI DEVICE, ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES
Charges
3280,341

Recent inspections

  • 1206824 (NAI Thu May 25 2023 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1049509 (NAI Fri Apr 13 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 969410 (NAI Mon Mar 09 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 817773 (NAI Fri Feb 08 2013 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources