FDA inspection
Lincotek Medical LLC.: FDA inspection ending Apr 28, 2015
FDA inspection 929478 · Voluntary Action Indicated (VAI) · Vandalia, OH
Key facts
| Inspection ID | 929478 |
|---|---|
| Firm | Lincotek Medical LLC. |
| FEI number | 3010039400 |
| Address | 811 Northwoods Blvd |
| City | Vandalia |
| State | OH |
| ZIP | 45377 |
| Country | United States |
| Fiscal year | 2015 |
| Inspection end date | Apr 28, 2015 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: 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