# Vanderbilt University Medical Center Human Research Protections Program, Nashville, TN – FDA Inspections

Source: https://www.keypedia.com/companies/vanderbilt-university-medical-center-human-research-protections-program/f8ee2728-0f4c-4be6-b3d6-373a01c2a2ed

> Inspection records and compliance data for Vanderbilt University Medical Center Human Research Protections Program in Nashville, Tennessee. 3 FDA inspections on record, last inspected September 01, 2022.

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## Details

- Name: Vanderbilt University Medical Center Human Research Protections Program
- FEI Number: 1043758
- Address Line 1: 3319 W End Ave Ste 600
- City: Nashville
- State: Tennessee
- Zip Code: 37203
- Country Name: United States
- Address: 3319 W End Ave Ste 600, Nashville, Tennessee 37203, United States
- Country: United States

## Related Documents

- FDA Inspection 1179812 - Vanderbilt University Medical Center Human Research Protections Program - 2022-09-01 — classification: No Action Indicated (NAI), source: FDA, date: September 1, 2022
- [FDA Inspection 1179812 - Vanderbilt University Medical Center Human Research Protections Program - 2022-09-01](https://www.keypedia.com/records/fda_inspections/vanderbilt-university-medical-center-human-research-protections-program/feddd2d2-3baa-45b4-a5ff-53ea24182454) — classification: No Action Indicated (NAI), source: FDA, date: September 1, 2022
- FDA Inspection 1179812 - Vanderbilt University Medical Center Human Research Protections Program - 2022-09-01 — classification: No Action Indicated (NAI), source: FDA, date: September 1, 2022
- FDA Inspection 948799 - Vanderbilt University Medical Center Human Research Protections Program - 2015-11-19 — classification: No Action Indicated (NAI), source: FDA, date: November 19, 2015
- [FDA Inspection 753168 - Vanderbilt University Medical Center Human Research Protections Program - 2011-11-02](https://www.keypedia.com/records/fda_inspections/vanderbilt-university-medical-center-human-research-protections-program/16a5d493-3054-4789-ae61-2cfd1c1aec1e) — classification: No Action Indicated (NAI), source: FDA, date: November 2, 2011

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