FDA Inspection 1315686 — Cardionet, LLC

Cardionet, LLC — FEI 3008773647

The FDA completed an inspection of Cardionet, LLC on April 16, 2026 in Phoenix, AZ. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
April 16, 2026
Fiscal Year
2026
Product Type
Devices
Project Area
Compliance: Devices
Location
Phoenix, AZ (United States)