FDA inspection
ARP Wave L.L.C.: FDA inspection ending Jun 9, 2008
FDA inspection 523007 · Voluntary Action Indicated (VAI) · Apple Valley, MN
Key facts
| Inspection ID | 523007 |
|---|---|
| Firm | ARP Wave L.L.C. |
| FEI number | 3004509773 |
| Address | 7721 145th St W |
| City | Apple Valley |
| State | MN |
| ZIP | 55124-7516 |
| Fiscal year | 2008 |
| Inspection end date | Jun 9, 2008 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: Med Devices |
| Product type | Devices |
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