FDA Inspection 1090126 — RadmediX LLC

RadmediX LLC — FEI 3009134655

The FDA completed an inspection of RadmediX LLC on April 16, 2019 in Moraine, OH. 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, 2019
Fiscal Year
2019
Product Type
Devices
Project Area
Compliance: Devices
Location
Moraine, OH (United States)