FDA Inspection 1080023 — DRE Medical Group Inc

DRE Medical Group Inc — FEI 1000122786

The FDA completed an inspection of DRE Medical Group Inc on February 21, 2019 in Louisville, KY. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
February 21, 2019
Fiscal Year
2019
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Louisville, KY (United States)

Citations

IDCFRDescription
337521 CFR 820.198(e)Records of complaint investigation