FDA-Inspected Site

RenovoRx, Inc.

2 FDA inspections are on record for RenovoRx, Inc. in Los Altos, United States.

483· Form 483 issued

Los Altos, United States · Last updated July 10, 2026

Overview

  • 2 FDA inspections are on record.
  • 1 inspection produced a Form 483.
  • The most recent recorded inspection date is 2022-04-04.

At a glance

Inspections

2

Form 483s

1

EIRs

0

Last outcome

Form 483

Inspection history

FDA inspections on record, most recent first.

InspectionCategoryOutcomeForm 483
30 Mar 2022 – 4 Apr 2022Medical Devices & Rad Health483View 483 →
17 May 2016 – 18 May 2016Medical Devices & Rad HealthClean

Observations on record

Form 483 observations cited at this site, most recent first.

4 Apr 2022
21 CFR 803.50(a)(1)

Report of Death or Serious Injury

Cited by Eileen M Malecki

4 Apr 2022
21 CFR 803.50(a)(1)

Report of Death or Serious Injury

Cited by Eileen M Malecki

4 Apr 2022
21 CFR 803.50(a)(1)

Report of Death or Serious Injury

Cited by Eileen M Malecki

4 Apr 2022
21 CFR 803.50(a)(1)

Report of Death or Serious Injury

Cited by Eileen M Malecki

Investigators

FDA investigators tied to this site in the record.

Recurring citations

CFR citation patterns observed across this site's inspections.

CitationWhat it coversCited
21 CFR 803.50(a)(1)Cited across public-safe Form 483 observations4x

Full site report

Get the verbatim findings behind RenovoRx, Inc.'s 1 Form 483

Recurring CFR citations, so your team knows what this site gets cited for.

  • The site's full inspection history, with every Form 483 and its outcome
  • Warning letters and recalls tied to the company behind it
  • Whether recurring CFR citations get closed out or repeat