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FDA Inspection 981961 — Glaukos Corporation

Glaukos Corporation — FEI 3012341472

The FDA completed an inspection of Glaukos Corporation on June 10, 2016 in San Clemente, 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
June 10, 2016
Fiscal Year
2016
Product Type
Devices
Project Area
Compliance: Devices
Location
San Clemente, CA (United States)

Facility

Other inspections at this facility

  • 1267669 (VAI Tue Apr 22 2025 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1251714 (NAI Thu Aug 15 2024 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1068254 (NAI Fri Aug 03 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 835427 (NAI Tue Jun 11 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 781289 (NAI Wed May 09 2012 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources