FDA inspection
Alera Technologies, Inc.: FDA inspection ending May 20, 2009
FDA inspection 583050 · Voluntary Action Indicated (VAI) · Salt Lake City, UT
Key facts
| Inspection ID | 583050 |
|---|---|
| Firm | Alera Technologies, Inc. |
| FEI number | 1719112 |
| Address | 2300 S Main St |
| City | Salt Lake City |
| State | UT |
| ZIP | 84115 |
| Country | United States |
| Fiscal year | 2009 |
| Inspection end date | May 20, 2009 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Drug Quality Assurance |
| 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