# Gallup Indian Medical Center Blood Bank, Gallup, NM – FDA Inspections

Source: https://www.keypedia.com/companies/gallup-indian-medical-center-blood-bank/53f91729-f4fc-464f-b74f-f2e7e5883119

> Inspection records and compliance data for Gallup Indian Medical Center Blood Bank in Gallup, New Mexico. 7 FDA inspections on record, last inspected August 19, 2025.

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## Details

- Name: Gallup Indian Medical Center Blood Bank
- FEI Number: 1672818
- Address Line 1: 516 E Nizhoni Blvd, Po Box 1337
- City: Gallup
- State: New Mexico
- Zip Code: 87301
- Country Name: United States
- Address: 516 E Nizhoni Blvd, Po Box 1337, Gallup, New Mexico 87301, United States
- Country: United States

## Related Documents

- FDA Inspection 1280402 - Gallup Indian Medical Center Blood Bank - 2025-08-19 — source: FDA, date: August 19, 2025
- FDA Inspection 1280402 - Gallup Indian Medical Center Blood Bank - 2025-08-19 — classification: No Action Indicated (NAI), source: FDA, date: August 19, 2025
- FDA Inspection 1118519 - Gallup Indian Medical Center Blood Bank - 2020-01-23 — classification: No Action Indicated (NAI), source: FDA, date: January 23, 2020
- FDA Inspection 1038140 - Gallup Indian Medical Center Blood Bank - 2017-11-28 — classification: No Action Indicated (NAI), source: FDA, date: November 28, 2017
- [FDA Inspection 967569 - Gallup Indian Medical Center Blood Bank - 2015-11-18](https://www.keypedia.com/records/fda_inspections/gallup-indian-medical-center-blood-bank/2849f00f-5396-491c-88d0-a59afadcdc32) — classification: Voluntary Action Indicated (VAI), source: FDA, date: November 18, 2015
- FDA Inspection 806066 - Gallup Indian Medical Center Blood Bank - 2012-10-04 — classification: No Action Indicated (NAI), source: FDA, date: October 4, 2012
- FDA Inspection 703524 - Gallup Indian Medical Center Blood Bank - 2010-12-16 — classification: No Action Indicated (NAI), source: FDA, date: December 16, 2010
- FDA Inspection 599865 - Gallup Indian Medical Center Blood Bank - 2009-07-27 — classification: No Action Indicated (NAI), source: FDA, date: July 27, 2009

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