FDA Inspection 1047149 — eScreen Inc

eScreen Inc — FEI 3003110749

The FDA completed an inspection of eScreen Inc on Apr 6, 2018 in Kansas City, MO. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Apr 6, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Compliance: Devices
Location
Kansas City, MO (United States)

Citations

IDCFRDescription
237121 CFR 820.30(a)Design control - no procedures