FDA Inspection 1232804 — Vivify Health, Inc.

Vivify Health, Inc. — FEI 3009896984

The FDA completed an inspection of Vivify Health, Inc. on Feb 23, 2024 in Eden Prairie, MN. 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). 2 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Feb 23, 2024
Fiscal Year
2024
Product Type
Devices
Project Area
Compliance: Devices
Location
Eden Prairie, MN (United States)

Citations

IDCFRDescription
367721 CFR 820.30(g)Design validation - software validation not performed
367821 CFR 820.30(g)Design Validation - Risk analysis not performed/inadequate