Home / Import refusals / AEK-2318343-4/1/1

FDA Import Refusal AEK-2318343-4/1/1 — ORCHID Orthopedic Solutions, Ltd.

ORCHID Orthopedic Solutions, Ltd. — FEI 3010089671

The FDA refused shipment AEK-2318343-4/1/1 from ORCHID Orthopedic Solutions, Ltd. (United Kingdom) on June 19, 2017. The refused product falls under Devices — PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, COATED, POLYMER/METAL/. Cited charge: 118 This firm has 3 other import refusals on record.

Refusal Details

Date
June 19, 2017
Country
United Kingdom
Product Category
Devices
Product Code
87MBH PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, COATED, POLYMER/METAL/
Charges
118

Recent inspections

  • 1014345 (NAI Thu May 11 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 871314 (NAI Thu Mar 20 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 716902 (VAI Thu Jan 27 2011 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 545242 (NAI Mon Oct 20 2008 00:00:00 GMT+0000 (Coordinated Universal Time))

Other import refusals

  • 799-0862032-5/1/1 (Fri Nov 08 2013 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • 799-0767907-4/1/1 (Fri Oct 25 2013 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • UPS-2911060-1/1/1 (Thu Dec 08 2011 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)

FDA data resources