# LifeSouth Community Blood Centers Shoals Region, Florence, AL – FDA Inspections

Source: https://www.keypedia.com/companies/lifesouth-community-blood-centers-shoals-region/d30f3111-1475-4e2a-9653-fc2cd58bfd2f

> Inspection records and compliance data for LifeSouth Community Blood Centers Shoals Region in Florence, Alabama. 7 FDA inspections on record, last inspected April 09, 2025.

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## Details

- Name: LifeSouth Community Blood Centers Shoals Region
- FEI Number: 3006497448
- Address Line 1: 307 Veterans Dr
- City: Florence
- State: Alabama
- Zip Code: 35630
- Country Name: United States
- Address: 307 Veterans Dr, Florence, Alabama 35630, United States
- Country: United States

## Related Documents

- FDA Inspection 1267799 - LifeSouth Community Blood Centers Shoals Region - 2025-04-09 — source: FDA, date: April 9, 2025
- FDA Inspection 1267799 - LifeSouth Community Blood Centers Shoals Region - 2025-04-09 — classification: No Action Indicated (NAI), source: FDA, date: April 9, 2025
- FDA Inspection 1100681 - LifeSouth Community Blood Centers Shoals Region - 2019-07-31 — classification: No Action Indicated (NAI), source: FDA, date: July 31, 2019
- FDA Inspection 1022907 - LifeSouth Community Blood Centers Shoals Region - 2017-07-12 — classification: No Action Indicated (NAI), source: FDA, date: July 12, 2017
- FDA Inspection 919067 - LifeSouth Community Blood Centers Shoals Region - 2015-03-20 — classification: No Action Indicated (NAI), source: FDA, date: March 20, 2015
- FDA Inspection 841646 - LifeSouth Community Blood Centers Shoals Region - 2013-07-18 — classification: No Action Indicated (NAI), source: FDA, date: July 18, 2013
- [FDA Inspection 744113 - LifeSouth Community Blood Centers Shoals Region - 2011-08-31](https://www.keypedia.com/records/fda_inspections/lifesouth-community-blood-centers-shoals-region/80d08f3d-3082-48ff-a11a-8ca40762219e) — classification: Voluntary Action Indicated (VAI), source: FDA, date: August 31, 2011
- FDA Inspection 588162 - LifeSouth Community Blood Centers Shoals Region - 2009-04-30 — classification: No Action Indicated (NAI), source: FDA, date: April 30, 2009

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