FDA inspection
ARL Biopharma, Inc. dba Analytical Research Laboratories: FDA inspection ending Mar 5, 2004
FDA inspection 317126 · Voluntary Action Indicated (VAI) · Oklahoma City, OK
Key facts
| Inspection ID | 317126 |
|---|---|
| Firm | ARL Biopharma, Inc. dba Analytical Research Laboratories |
| FEI number | 3003644883 |
| Address | 840 Research Pkwy Ste 546 |
| City | Oklahoma City |
| State | OK |
| ZIP | 73104-3697 |
| Fiscal year | 2004 |
| Inspection end date | Mar 5, 2004 |
| 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