FDA Inspection 781289 — Glaukos Corporation
The FDA completed an inspection of Glaukos Corporation on May 9, 2012 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
- May 9, 2012
- Fiscal Year
- 2012
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- San Clemente, CA (United States)