FDA inspection
Avera Home Medical Equipment: FDA inspection ending Feb 23, 2000
FDA inspection 14595 · Voluntary Action Indicated (VAI) · Sioux Falls, SD
Key facts
| Inspection ID | 14595 |
|---|---|
| Firm | Avera Home Medical Equipment |
| FEI number | 1000150331 |
| Address | 2400 S Minnesota Ave Ste 102 |
| City | Sioux Falls |
| State | SD |
| ZIP | 57105-3706 |
| Fiscal year | 2000 |
| Inspection end date | Feb 23, 2000 |
| Classification | Voluntary Action Indicated (VAI) |
| 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