FDA Inspection
RenovoRx, Inc.RenovoRx, Inc. – FDA Inspection, Apr 4, 2022
Record Details
This FDA Inspection record concerns RenovoRx, Inc., with an inspection on April 4, 2022, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- RenovoRx, Inc.
- Inspection Date
- April 4, 2022
- Product Type
- Devices
View Company Profile
ID · a3744e11-0422-4793-b1f6-94995dbbc6b9
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1166306
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
1- 21 CFR 803.50(a)(1)Report of Death or Serious Injury
Full citation text and observation details available on the Dashboard.
Other FDA inspections of RenovoRx, Inc.
2| Date | Classification | Office | Project area |
|---|---|---|---|
| June 16, 2026 | Not classified | San Francisco District Office | |
| May 18, 2016 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for RenovoRx, Inc.
- FDA Inspection 1324452 - 2026-06-16
- FDA Inspection 978263 - 2016-05-18
Document or profile
One record shows the event. A profile shows the pattern.
Buy this document for the source file and details behind this single event.
Choose full profile access to connect related records, sites, people, citations, and enforcement history in one view.