FDA inspection
LED Technologies, LLC: FDA inspection ending Jun 30, 2016
FDA inspection 981430 · Voluntary Action Indicated (VAI) · Greenwood Village, CO
Key facts
| Inspection ID | 981430 |
|---|---|
| Firm | LED Technologies, LLC |
| FEI number | 3006315288 |
| Address | 6000 Greenwood Plaza Blvd Ste 110 |
| City | Greenwood Village |
| State | CO |
| ZIP | 80111 |
| Country | United States |
| Fiscal year | 2016 |
| Inspection end date | Jun 30, 2016 |
| 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