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FDA Inspection 1068254 — Glaukos Corporation

Glaukos Corporation — FEI 3012341472

The FDA completed an inspection of Glaukos Corporation on August 3, 2018 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
August 3, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
San Clemente, CA (United States)

Additional Details

Sponsor, Contract Research Organization

Facility

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  • 835427 (NAI Tue Jun 11 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
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FDA data resources