FDA inspection
Lincotek Medical LLC.: FDA inspection ending Sep 26, 2024
FDA inspection 1250228 · Voluntary Action Indicated (VAI) · Vandalia, OH
Key facts
| Inspection ID | 1250228 |
|---|---|
| Firm | Lincotek Medical LLC. |
| FEI number | 3010039400 |
| Address | 811 Northwoods Blvd |
| City | Vandalia |
| State | OH |
| ZIP | 45377 |
| Country | United States |
| Fiscal year | 2024 |
| Inspection end date | Sep 26, 2024 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Postmarket Assurance: 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