FDA inspection
UnityPoint At Home: FDA inspection ending Feb 14, 2002
FDA inspection 203894 · Official Action Indicated (OAI) · Urbandale, IA
Key facts
| Inspection ID | 203894 |
|---|---|
| Firm | UnityPoint At Home |
| FEI number | 1931164 |
| Address | 11333 Aurora Ave |
| City | Urbandale |
| State | IA |
| ZIP | 50322-7908 |
| Fiscal year | 2002 |
| Inspection end date | Feb 14, 2002 |
| Classification | Official Action Indicated (OAI) |
| Project area | Drug Quality Assurance |
| 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
- 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