FDA Inspection 1247935 — Verily LIfe Sciences LLC

Verily LIfe Sciences LLC — FEI 3013170399

The FDA completed an inspection of Verily LIfe Sciences LLC on Aug 30, 2024 in San Bruno, CA. 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
Aug 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

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.