FDA Inspection 1335282 — GRAIL, Inc.

GRAIL, Inc. — FEI 3013103906

The FDA completed an inspection of GRAIL, Inc. on Aug 31, 2026 in Menlo Park, 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
Aug 31, 2026
Fiscal Year
2026
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Menlo Park, CA (United States)

Additional Details

Sponsor, Contract Research Organization

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