# FDA Inspection 978263 - RenovoRx, Inc. - May 18, 2016

Source: https://www.keypedia.com/records/fda_inspections/renovorx-inc/427d1984-cb43-4361-9c81-b3e02f83351d
Source feed: FDA_Inspections

> FDA Inspection 978263 for RenovoRx, Inc. on May 18, 2016. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 978263
- Company Name: RenovoRx, Inc.
- Inspection Date: 2016-05-18
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.keypedia.com/companies/renovorx-inc/53ed9d73-0643-4791-8e37-cd5a04c834fd

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7