FDA inspection
Veritas Laboratories Inc: FDA inspection ending Oct 20, 2003
FDA inspection 299350 · No Action Indicated (NAI) · Burlington, NC
Key facts
| Inspection ID | 299350 |
|---|---|
| Firm | Veritas Laboratories Inc |
| FEI number | 1053373 |
| Address | 239 E Front St |
| City | Burlington |
| State | NC |
| ZIP | 27215-5879 |
| Fiscal year | 2004 |
| Inspection end date | Oct 20, 2003 |
| Classification | No Action Indicated (NAI) |
| Project area | Bio-Research Monit: Human Drugs |
| Product type | Drugs |
At a glance
- None Citations
- None 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