FDA Inspection 1251714 — Glaukos Corporation

Glaukos Corporation — FEI 3012341472

The FDA completed an inspection of Glaukos Corporation on August 15, 2024 in San Clemente, CA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
August 15, 2024
Fiscal Year
2024
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
San Clemente, CA (United States)

Additional Details

Postmarket Adverse Drug Experience (PADE)