Inspection classificationInspection ended May 18, 2026

FDA inspection of GRAIL, Inc.: VAI

Voluntary action indicated

FDA's record ↗

FDA classified an inspection of GRAIL, Inc. in Menlo Park, CA as VAI (voluntary action indicated). The inspection ended on May 18, 2026. Product type: Devices.

On the record

Establishment
GRAIL, Inc.
Location
Menlo Park, CA
Classification
VAI · Voluntary action indicated
Inspection ended
2026-05-18
Product type
Devices
Fiscal year
FY2026
FDA establishment identifier (FEI)
3013103906
Source
FDA Data Dashboard ↗

The full record

An account shows the project areas inspected and whether citations were posted.

What an inspection classification is

After an inspection FDA classifies the outcome. NAI (no action indicated): no objectionable conditions were found, or none that justify further action. VAI (voluntary action indicated): objectionable conditions were found, but the agency is not prepared to take or recommend regulatory action. OAI (official action indicated): regulatory or administrative action is recommended.

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From FDA Data Dashboard; FDA posts a classification after its review, which can be months after the inspection ended. The record may have changed since it was read.

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