# LifeSouth Community Blood Centers, Inc. - Marshall Region, Albertville, AL – FDA Inspections

Source: https://www.keypedia.com/companies/lifesouth-community-blood-centers-inc-marshall-region/3b26d623-aa5e-43b3-b546-9aaac0873167

> Inspection records and compliance data for LifeSouth Community Blood Centers, Inc. - Marshall Region in Albertville, Alabama. 7 FDA inspections on record, last inspected September 08, 2025.

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## Details

- Name: LifeSouth Community Blood Centers, Inc. - Marshall Region
- FEI Number: 3003972293
- Address Line 1: 8626 US Highway 431
- City: Albertville
- State: Alabama
- Zip Code: 35950
- Country Name: United States
- Address: 8626 US Highway 431, Albertville, Alabama 35950, United States
- Country: United States

## Related Documents

- FDA Inspection 1281972 - LifeSouth Community Blood Centers, Inc. - Marshall Region - 2025-09-08 — source: FDA, date: September 8, 2025
- FDA Inspection 1281972 - LifeSouth Community Blood Centers, Inc. - Marshall Region - 2025-09-08 — classification: No Action Indicated (NAI), source: FDA, date: September 8, 2025
- FDA Inspection 1207308 - LifeSouth Community Blood Centers, Inc. - Marshall Region - 2023-05-31 — classification: No Action Indicated (NAI), source: FDA, date: May 31, 2023
- FDA Inspection 1054918 - LifeSouth Community Blood Centers, Inc. - Marshall Region - 2018-04-23 — classification: No Action Indicated (NAI), source: FDA, date: April 23, 2018
- FDA Inspection 971031 - LifeSouth Community Blood Centers, Inc. - Marshall Region - 2016-05-10 — classification: No Action Indicated (NAI), source: FDA, date: May 10, 2016
- FDA Inspection 889730 - LifeSouth Community Blood Centers, Inc. - Marshall Region - 2014-07-30 — classification: No Action Indicated (NAI), source: FDA, date: July 30, 2014
- FDA Inspection 792599 - LifeSouth Community Blood Centers, Inc. - Marshall Region - 2012-07-26 — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 26, 2012
- FDA Inspection 674006 - LifeSouth Community Blood Centers, Inc. - Marshall Region - 2010-06-30 — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 30, 2010

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