FDA inspection

RenovoRx, Inc.: FDA inspection ending Apr 4, 2022

FDA inspection 1166306 · Voluntary Action Indicated (VAI) · Mountain View, CA

Key facts

Inspection ID 1166306
Firm RenovoRx, Inc.
FEI number 3011279674
Address 4546 El Camino Real Ste B1
City Mountain View
State CA
ZIP 94040
Country United States
Fiscal year 2022
Inspection end date Apr 4, 2022
Classification Voluntary Action Indicated (VAI)
Project area Compliance: Devices
Product type Devices

At a glance

  • 1–9 Citations
  • 1–9 Posted citations
  • No Warning letter followed
  • Yes Form FDA 483 issued
  • No Establishment inspection report (EIR) exists
  • 1–9 Inspections at this FEI

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About FDA inspections

FDA inspections are classified as No Action Indicated (NAI), Voluntary Action Indicated (VAI) or Official Action Indicated (OAI). Inspections of individual clinical investigators are not published here.

Source: U.S. Food and Drug Administration (FDA), inspection classification data

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