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FDA Inspection 961858 — EKOS Corporation

EKOS Corporation — FEI 3001627457

The FDA completed an inspection of EKOS Corporation on December 18, 2015 in Bothell, WA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
December 18, 2015
Fiscal Year
2016
Product Type
Devices
Project Area
Compliance: Devices
Location
Bothell, WA (United States)

Facility

Other inspections at this facility

  • 1107256 (NAI Thu Sep 26 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 853324 (NAI Wed Oct 30 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 719863 (NAI Fri Apr 01 2011 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 589006 (NAI Tue May 19 2009 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources