FDA inspection
Avedro, a Glaukos Company: FDA inspection ending Jun 26, 2025
FDA inspection 1275997 · Burlington, MA
Key facts
| Inspection ID | 1275997 |
|---|---|
| Firm | Avedro, a Glaukos Company |
| FEI number | 3007851054 |
| Address | 30 North Ave |
| City | Burlington |
| State | MA |
| ZIP | 01803-3327 |
| Fiscal year | 2025 |
| Inspection end date | Jun 26, 2025 |
| Project area | Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Postmarket Assurance: Medical Devices|Radiation Control and Health Safety Act (RCHSA) Authority|Postmarket Assurance: Medical Devices|Radiation Control and Health Safety Act (RCHSA) Authority|Postmarket Assurance: Medical Devices|Radiation Control and Health Safety Act (RCHSA) Authority|Postmarket Assurance: Medical Devices|Radiation Control and Health Safety Act (RCHSA) Authority|Postmarket Assurance: Medical Devices|Radiation Control and Health Safety Act (RCHSA) Authority|Postmarket Assurance: Medical Devices|Radiation Control and Health Safety Act (RCHSA) Authority|Postmarket Assurance: Medical Devices|Radiation Control and Health Safety Act (RCHSA) Authority|Postmarket Assurance: Medical Devices|Radiation Control and Health Safety Act (RCHSA) Authority|Postmarket Assurance: Medical Devices|Radiation Control and Health Safety Act (RCHSA) Authority|Postmarket Assurance: Medical Devices|Radiation Control and Health Safety Act (RCHSA) Authority|Postmarket Assurance: Medical Devices|Radiation Control and Health Safety Act (RCHSA) Authority|Postmarket Assurance: Medical Devices|Radiation Control and Health Safety Act (RCHSA) Authority|Postmarket Assurance: Medical Devices|Radiation Control and Health Safety Act (RCHSA) Authority|Postmarket Assurance: Medical Devices|Radiation Control and Health Safety Act (RCHSA) Authority|Postmarket Assurance: Medical Devices|Radiation Control and Health Safety Act (RCHSA) Authority|Postmarket Assurance: Medical Devices|Radiation Control and Health Safety Act (RCHSA) Authority|Postmarket Assurance: Medical Devices|Radiation Control and Health Safety Act (RCHSA) Authority|Postmarket Assurance: Medical Devices|Radiation Control and Health Safety Act (RCHSA) Authority|Postmarket Assurance: Medical Devices|Radiation Control and Health Safety Act (RCHSA) Authority|Postmarket Assurance: Medical Devices|Radiation Control and Health Safety Act (RCHSA) Authority|Postmarket Assurance: Medical Devices|Radiation Control and Health Safety Act (RCHSA) Authority|Postmarket Assurance: Medical Devices|Radiation Control and Health Safety Act (RCHSA) Authority|Postmarket Assurance: Medical Devices|Radiation Control and Health Safety Act (RCHSA) Authority|Postmarket Assurance: Medical Devices|Radiation Control and Health Safety Act (RCHSA) Authority|Postmarket Assurance: Medical Devices|Radiation Control and Health Safety Act (RCHSA) Authority|Postmarket Assurance: Medical Devices|Radiation Control and Health Safety Act (RCHSA) Authority|Postmarket Assurance: Medical Devices|Radiation Control and Health Safety Act (RCHSA) Authority|Postmarket Assurance: Medical Devices|Radiation Control and Health Safety Act (RCHSA) Authority|Postmarket Assurance: Medical Devices|Radiation Control and Health Safety Act (RCHSA) Authority|Postmarket Assurance: Medical Devices|Radiation Control and Health Safety Act (RCHSA) Authority|Postmarket Assurance: Medical Devices|Radiation Control and Health Safety Act (RCHSA) Authority|Postmarket Assurance: Medical Devices|Radiation Control and Health Safety Act (RCHSA) Authority|Postmarket Assurance: Medical Devices|Radiation Control and Health Safety Act (RCHSA) Authority|Postmarket Assurance: Medical Devices|Radiation Control and Health Safety Act (RCHSA) Authority|Postmarket Assurance: Medical Devices|Radiation Control and Health Safety Act (RCHSA) Authority|Postmarket Assurance: Medical Devices|Radiation Control and Health Safety Act (RCHSA) Authority|Postmarket Assurance: Medical Devices|Radiation Control and Health Safety Act (RCHSA) Authority|Postmarket Assurance: Medical Devices|Radiation Control and Health Safety Act (RCHSA) Authority|Postmarket Assurance: Medical Devices|Radiation Control and Health Safety Act (RCHSA) Authority|Postmarket Assurance: Medical Devices|Radiation Control and Health Safety Act (RCHSA) Authority|Postmarket Assurance: Medical Devices|Radiation Control and Health Safety Act (RCHSA) Authority|Postmarket Assurance: Medical Devices|Radiation Control and Health Safety Act (RCHSA) Authority|Postmarket Assurance: Medical Devices|Radiation Control and Health Safety Act (RCHSA) Authority|Postmarket Assurance: Medical Devices|Radiation Control and Health Safety Act (RCHSA) Authority|Postmarket Assurance: Medical Devices|Radiation Control and Health Safety Act (RCHSA) Authority|Postmarket Assurance: Medical Devices|Radiation Control and Health Safety Act (RCHSA) Authority |
| Product type | Devices |
At a glance
- 1–9 Citations
- 1–9 Posted citations
- No Warning letter followed
- Yes Form FDA 483 issued
- No Establishment inspection report (EIR) exists
- 1–9 Inspections at this FEI
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA inspections
FDA inspections are classified as No Action Indicated (NAI), Voluntary Action Indicated (VAI) or Official Action Indicated (OAI). Inspections of individual clinical investigators are not published here.
Source: U.S. Food and Drug Administration (FDA), inspection classification data