FDA Inspection 562763 — Glaukos Corporation
The FDA completed an inspection of Glaukos Corporation on March 9, 2009 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
- March 9, 2009
- Fiscal Year
- 2009
- Product Type
- Devices
- Project Area
- Bioresearch Monitoring
- Location
- San Clemente, CA (United States)
Additional Details
Sponsor, Contract Research Organization