FDA Inspection 1310624 — Intravu, Inc.

Intravu, Inc. — FEI 3014202166

The FDA completed an inspection of Intravu, Inc. on Apr 2, 2026 in Redwood City, 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
Apr 2, 2026
Fiscal Year
2026
Product Type
Devices
Project Area
Compliance: Devices
Location
Redwood City, CA (United States)

Citations

IDCFRDescription
23085ISO 13485:2016 Clause 7.1Processes needed for product realization not planned and developed

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