# Missouri Baptist Medical Center Blood Bank, Saint Louis, MO – FDA Inspections

Source: https://www.keypedia.com/companies/missouri-baptist-medical-center-blood-bank/af371481-23be-4369-8a3f-a662647298ea

> Inspection records and compliance data for Missouri Baptist Medical Center Blood Bank in Saint Louis, Missouri. 7 FDA inspections on record, last inspected October 22, 2024.

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## Details

- Name: Missouri Baptist Medical Center Blood Bank
- FEI Number: 1973195
- Address Line 1: 3015 N Ballas Rd
- City: Saint Louis
- State: Missouri
- Zip Code: 63131
- Country Name: United States
- Address: 3015 N Ballas Rd, Saint Louis, Missouri 63131, United States
- Country: United States

## Related Documents

- FDA Inspection 1252556 - Missouri Baptist Medical Center Blood Bank - 2024-10-22 — source: FDA, date: October 22, 2024
- FDA Inspection 1252556 - Missouri Baptist Medical Center Blood Bank - 2024-10-22 — classification: No Action Indicated (NAI), source: FDA, date: October 22, 2024
- FDA Inspection 1170380 - Missouri Baptist Medical Center Blood Bank - 2022-05-13 — classification: No Action Indicated (NAI), source: FDA, date: May 13, 2022
- FDA Inspection 1170380 - Missouri Baptist Medical Center Blood Bank - 2022-05-13 — classification: No Action Indicated (NAI), source: FDA, date: May 13, 2022
- FDA Inspection 1057943 - Missouri Baptist Medical Center Blood Bank - 2018-06-11 — classification: No Action Indicated (NAI), source: FDA, date: June 11, 2018
- FDA Inspection 972934 - Missouri Baptist Medical Center Blood Bank - 2016-05-25 — classification: No Action Indicated (NAI), source: FDA, date: May 25, 2016
- FDA Inspection 858536 - Missouri Baptist Medical Center Blood Bank - 2013-12-10 — classification: No Action Indicated (NAI), source: FDA, date: December 10, 2013
- FDA Inspection 753797 - Missouri Baptist Medical Center Blood Bank - 2011-11-16 — classification: No Action Indicated (NAI), source: FDA, date: November 16, 2011
- FDA Inspection 639011 - Missouri Baptist Medical Center Blood Bank - 2010-01-15 — classification: No Action Indicated (NAI), source: FDA, date: January 15, 2010

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