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FDA Inspection 835427 — Glaukos Corporation

Glaukos Corporation — FEI 3012341472

The FDA completed an inspection of Glaukos Corporation on June 11, 2013 in San Clemente, CA. 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
June 11, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Compliance: Devices
Location
San Clemente, CA (United States)

Facility

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FDA data resources