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FDA Inspection 714014 — Iridex Corporation

Iridex Corporation — FEI 2939653

The FDA completed an inspection of Iridex Corporation on March 17, 2011 in Mountain View, CA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
March 17, 2011
Fiscal Year
2011
Product Type
Devices
Project Area
Compliance: Devices
Location
Mountain View, CA (United States)

Facility

Other inspections at this facility

  • 1218928 (NAI Wed Sep 20 2023 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 988542 (NAI Fri Aug 19 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 906286 (VAI Tue Dec 02 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 836353 (VAI Wed Jul 10 2013 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources