FDA inspection
Resmed Corporation: FDA inspection ending Feb 23, 2009
FDA inspection 564987 · Voluntary Action Indicated (VAI) · San Diego, CA
Key facts
| Inspection ID | 564987 |
|---|---|
| Firm | Resmed Corporation |
| FEI number | 1000115734 |
| Address | 9001 Spectrum Center Blvd |
| City | San Diego |
| State | CA |
| ZIP | 92123 |
| Country | United States |
| Fiscal year | 2009 |
| Inspection end date | Feb 23, 2009 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Postmarket Assurance: Devices |
| Product type | Devices |
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