FDA inspection
Lightbody Medical Technologies Inc: FDA inspection ending Nov 2, 2011
FDA inspection 753736 · No Action Indicated (NAI) · Burr Ridge, IL
Key facts
| Inspection ID | 753736 |
|---|---|
| Firm | Lightbody Medical Technologies Inc |
| FEI number | 3007048062 |
| Address | 101 Tower Dr |
| City | Burr Ridge |
| State | IL |
| ZIP | 60527 |
| Country | United States |
| Fiscal year | 2012 |
| Inspection end date | Nov 2, 2011 |
| Classification | No Action Indicated (NAI) |
| Project area | Human Cellular, Tissue, and Gene Therapies |
| Product type | Biologics |
At a glance
- None Citations
- None Posted citations
- No Warning letter followed
- No 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