FDA Inspection 1045173 — Sonogage Inc

Sonogage Inc — FEI 1526843

The FDA completed an inspection of Sonogage Inc on March 21, 2018 in Cleveland, OH. 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 21, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Cleveland, OH (United States)

Citations

IDCFRDescription
368021 CFR 820.70(a)Process control procedures, Lack of or inadequate procedures