FDA inspection
SpineCraft, LLC.: FDA inspection ending Mar 22, 2024
FDA inspection 1233747 · Voluntary Action Indicated (VAI) · Westmont, IL
Key facts
| Inspection ID | 1233747 |
|---|---|
| Firm | SpineCraft, LLC. |
| FEI number | 3004717358 |
| Address | 777 Oakmont Ln Ste 200 |
| City | Westmont |
| State | IL |
| ZIP | 60559 |
| Country | United States |
| Fiscal year | 2024 |
| Inspection end date | Mar 22, 2024 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: Devices |
| 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