FDA Inspection 1084308 — SonarMed Inc

SonarMed Inc — FEI 3009923584

The FDA completed an inspection of SonarMed Inc on March 29, 2019 in Carmel, IN. 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
March 29, 2019
Fiscal Year
2019
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Carmel, IN (United States)

Citations

IDCFRDescription
319221 CFR 820.30(g)Design validation - user needs and intended uses