FDA Inspection 1247935 — Verily LIfe Sciences LLC

Verily LIfe Sciences LLC — FEI 3013170399

The FDA completed an inspection of Verily LIfe Sciences LLC on August 30, 2024 in San Bruno, CA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
August 30, 2024
Fiscal Year
2024
Product Type
Devices
Project Area
Compliance: Devices
Location
San Bruno, CA (United States)

Citations

IDCFRDescription
313021 CFR 820.100(a)Lack of or inadequate procedures