FDA inspection
Resmed Corporation: FDA inspection ending Jan 13, 2016
FDA inspection 998736 · Voluntary Action Indicated (VAI) · San Diego, CA
Key facts
| Inspection ID | 998736 |
|---|---|
| Firm | Resmed Corporation |
| FEI number | 1000115734 |
| Address | 9001 Spectrum Center Blvd |
| City | San Diego |
| State | CA |
| ZIP | 92123-1438 |
| Fiscal year | 2016 |
| Inspection end date | Jan 13, 2016 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: Medical 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