FDA Inspection 562763 — Glaukos Corporation
The FDA completed an inspection of Glaukos Corporation on Mar 9, 2009 in San Clemente, CA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Devices.
Inspection details
- Classification
- Voluntary Action Indicated (VAI)
- End Date
- Mar 9, 2009
- Fiscal Year
- 2009
- Product Type
- Devices
- Project Area
- Bioresearch Monitoring
- Location
- San Clemente, CA (United States)
Additional details
Sponsor, Contract Research Organization