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FDA Inspection 800085 — Gynex Corporation

Gynex Corporation — FEI 3001238683

The FDA completed an inspection of Gynex Corporation on September 21, 2012 in Redmond, 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
September 21, 2012
Fiscal Year
2012
Product Type
Devices
Project Area
Compliance: Devices
Location
Redmond, WA (United States)

Facility

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  • 975324 (NAI Fri May 27 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 876242 (NAI Fri Apr 25 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 791097 (NAI Fri Jul 20 2012 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 645081 (VAI Thu Jan 21 2010 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources