FDA inspection
Intertek USA Inc.: FDA inspection ending Jan 21, 2013
FDA inspection 815726 · No Action Indicated (NAI) · Whitehouse, NJ
Key facts
| Inspection ID | 815726 |
|---|---|
| Firm | Intertek USA Inc. |
| FEI number | 1000151295 |
| Address | 291 Route 22 East |
| City | Whitehouse |
| State | NJ |
| ZIP | 08888 |
| Country | United States |
| Fiscal year | 2013 |
| Inspection end date | Jan 21, 2013 |
| Classification | No Action Indicated (NAI) |
| Project area | Drug Quality Assurance |
| Product type | Drugs |
At a glance
- None Citations
- None Posted citations
- No Warning letter followed
- No Form FDA 483 issued
- No Establishment inspection report (EIR) exists
- 10–99 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