Home / Import refusals / 799-5078126-5/1/1

FDA Import Refusal 799-5078126-5/1/1 — OmniLife Science

OmniLife Science — FEI 3008342029

The FDA refused shipment 799-5078126-5/1/1 from OmniLife Science (United States) on April 8, 2016. The refused product falls under Devices — ORTHOPEDIC STEREOTAXIC INSTRUMENT. Cited charges: 118,3280 This firm has 2 other import refusals on record.

Refusal Details

Date
April 8, 2016
Country
United States
Product Category
Devices
Product Code
87OLO ORTHOPEDIC STEREOTAXIC INSTRUMENT
Charges
118,3280

Recent inspections

  • 1166323 (NAI Mon Apr 04 2022 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1025556 (NAI Wed Sep 13 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 810557 (VAI Thu Dec 06 2012 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 713580 (NAI Thu Feb 03 2011 00:00:00 GMT+0000 (Coordinated Universal Time))

Other import refusals

  • 799-5051951-7/1/1 (Fri Apr 08 2016 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • AEK-6405721-5/1/1 (Fri Aug 20 2004 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)

FDA data resources