FDA Inspection 1167119 — ResMed Corp

ResMed Corp — FEI 3011205710

The FDA completed an inspection of ResMed Corp on Mar 4, 2022 in Lithia Springs, GA. 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
Mar 4, 2022
Fiscal Year
2022
Product Type
Devices
Project Area
Compliance: Devices
Location
Lithia Springs, GA (United States)