Home / Import refusals / 799-2363444-8/11/8

FDA Import Refusal 799-2363444-8/11/8 — NuVasive Inc

NuVasive Inc — FEI 3002980729

The FDA refused shipment 799-2363444-8/11/8 from NuVasive Inc (United States) on January 12, 2023. The refused product falls under Devices — ORTHOPEDIC MANUAL SURGICAL INSTRUMENT. Cited charges: 118,3280 This firm has 5 or more other import refusals on record.

Refusal Details

Date
January 12, 2023
Country
United States
Product Category
Devices
Product Code
87LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT
Charges
118,3280

Recent inspections

  • 1011810 (NAI Fri May 26 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 904804 (NAI Wed Nov 19 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 865024 (NAI Wed Feb 05 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 805149 (OAI Fri Nov 02 2012 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 768996 (NAI Fri Feb 10 2012 00:00:00 GMT+0000 (Coordinated Universal Time))

Compliance actions

Other import refusals

  • 799-2363444-8/11/18 (Thu Jan 12 2023 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • 799-2363444-8/11/26 (Thu Jan 12 2023 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • 799-2363444-8/11/1 (Thu Jan 12 2023 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • 799-2363444-8/11/2 (Thu Jan 12 2023 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • 799-2363444-8/11/4 (Thu Jan 12 2023 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)

FDA data resources