FDA inspection
Litron Laboratories: FDA inspection ending Jun 2, 2009
FDA inspection 590995 · Voluntary Action Indicated (VAI) · Rochester, NY
Key facts
| Inspection ID | 590995 |
|---|---|
| Firm | Litron Laboratories |
| FEI number | 3002600600 |
| Address | 3500 Winton Pl Ste 1B |
| City | Rochester |
| State | NY |
| ZIP | 14623-2860 |
| Fiscal year | 2009 |
| Inspection end date | Jun 2, 2009 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Bio-Research Monit: Human Drugs |
| Product type | Drugs |
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