FDA inspection
EXL Laboratories, LLC.: FDA inspection ending Jun 5, 2000
FDA inspection 25530 · Official Action Indicated (OAI) · Minneapolis, MN
Key facts
| Inspection ID | 25530 |
|---|---|
| Firm | EXL Laboratories, LLC. |
| FEI number | 2127526 |
| Address | 1001 Glenwood Ave |
| City | Minneapolis |
| State | MN |
| ZIP | 55405-1429 |
| Fiscal year | 2000 |
| Inspection end date | Jun 5, 2000 |
| Classification | Official Action Indicated (OAI) |
| Project area | Monit of Marketed Animal Drug,Feed &Dev |
| Product type | Drugs |
At a glance
- None Citations
- 1–9 Posted citations
- No Warning letter followed
- Yes 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