FDA Inspection 714766 — ResMed Ltd.
The FDA completed an inspection of ResMed Ltd. on Feb 3, 2011 in Bella Vista. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.
Inspection details
- Classification
- No Action Indicated (NAI)
- End Date
- Feb 3, 2011
- Fiscal Year
- 2011
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Bella Vista (Australia)