FDA inspection
Relign Corp: FDA inspection ending May 17, 2023
FDA inspection 1206399 · Voluntary Action Indicated (VAI) · Campbell, CA
Key facts
| Inspection ID | 1206399 |
|---|---|
| Firm | Relign Corp |
| FEI number | 3012790575 |
| Address | 655 Campbell Technology Pkwy Ste 275 |
| City | Campbell |
| State | CA |
| ZIP | 95008 |
| Country | United States |
| Fiscal year | 2023 |
| Inspection end date | May 17, 2023 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Postmarket Assurance: Devices |
| Product type | Devices |
At a glance
- None 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