FDA Inspection 1028629 — Verily LIfe Sciences LLC

Verily LIfe Sciences LLC — FEI 3013170399

The FDA completed an inspection of Verily LIfe Sciences LLC on Sep 7, 2017 in San Bruno, CA. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Sep 7, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
San Bruno, CA (United States)

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