# North Mississippi Medical Center Blood Bank, Tupelo, MS – FDA Inspections

Source: https://www.keypedia.com/companies/north-mississippi-medical-center-blood-bank/68c3db42-8199-464e-8c9c-4edf7ffef8a3

> Inspection records and compliance data for North Mississippi Medical Center Blood Bank in Tupelo, Mississippi. 7 FDA inspections on record, last inspected January 17, 2025.

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## Details

- Name: North Mississippi Medical Center Blood Bank
- FEI Number: 1072776
- Address Line 1: 830 S Gloster St
- City: Tupelo
- State: Mississippi
- Zip Code: 38801
- Country Name: United States
- Address: 830 S Gloster St, Tupelo, Mississippi 38801, United States
- Country: United States

## Related Documents

- FDA Inspection 1258991 - North Mississippi Medical Center Blood Bank - 2025-01-17 — source: FDA, date: January 17, 2025
- FDA Inspection 1258991 - North Mississippi Medical Center Blood Bank - 2025-01-17 — classification: No Action Indicated (NAI), source: FDA, date: January 17, 2025
- FDA Inspection 1122937 - North Mississippi Medical Center Blood Bank - 2020-03-03 — classification: No Action Indicated (NAI), source: FDA, date: March 3, 2020
- FDA Inspection 1122937 - North Mississippi Medical Center Blood Bank - 2020-03-03 — classification: No Action Indicated (NAI), source: FDA, date: March 3, 2020
- FDA Inspection 1067791 - North Mississippi Medical Center Blood Bank - 2018-09-20 — classification: No Action Indicated (NAI), source: FDA, date: September 20, 2018
- FDA Inspection 972950 - North Mississippi Medical Center Blood Bank - 2016-06-16 — classification: No Action Indicated (NAI), source: FDA, date: June 16, 2016
- FDA Inspection 846565 - North Mississippi Medical Center Blood Bank - 2013-08-01 — classification: No Action Indicated (NAI), source: FDA, date: August 1, 2013
- FDA Inspection 730384 - North Mississippi Medical Center Blood Bank - 2011-06-09 — classification: No Action Indicated (NAI), source: FDA, date: June 9, 2011
- FDA Inspection 574455 - North Mississippi Medical Center Blood Bank - 2009-04-07 — classification: No Action Indicated (NAI), source: FDA, date: April 7, 2009

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