FDA inspection
ResMed Corp: FDA inspection ending Jan 21, 2016
FDA inspection 998732 · No Action Indicated (NAI) · Lithia Springs, GA
Key facts
| Inspection ID | 998732 |
|---|---|
| Firm | ResMed Corp |
| FEI number | 3011205710 |
| Address | 600 Riverside Pkwy Ste 100 |
| City | Lithia Springs |
| State | GA |
| ZIP | 30122-3893 |
| Fiscal year | 2016 |
| Inspection end date | Jan 21, 2016 |
| Classification | No Action Indicated (NAI) |
| Project area | Compliance: Medical Devices |
| Product type | Devices |
At a glance
- None Citations
- None 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