FDA Inspection 1280924 — Rhythmedix LLC

Rhythmedix LLC — FEI 3011265784

The FDA completed an inspection of Rhythmedix LLC on August 22, 2025 in Mount Laurel, NJ. 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
August 22, 2025
Fiscal Year
2025
Product Type
Devices
Project Area
Compliance: Devices
Location
Mount Laurel, NJ (United States)