FDA Inspection 1267669 — Glaukos Corporation

Glaukos Corporation — FEI 3012341472

The FDA completed an inspection of Glaukos Corporation on April 22, 2025 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). 1 citation was issued during this inspection. Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
April 22, 2025
Fiscal Year
2025
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
San Clemente, CA (United States)

Citations

IDCFRDescription
202721 CFR 211.192Investigations of discrepancies, failures