# LifeSouth Community Blood Centers, Inc., Brooksville, FL – FDA Inspections

Source: https://www.keypedia.com/companies/lifesouth-community-blood-centers-inc/0c59d804-15e8-4446-a160-0dc15da79070

> Inspection records and compliance data for LifeSouth Community Blood Centers, Inc. in Brooksville, Florida. 7 FDA inspections on record, last inspected February 24, 2026.

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## Details

- Name: LifeSouth Community Blood Centers, Inc.
- FEI Number: 1038804
- Address Line 1: 12395 Cortez Blvd
- City: Brooksville
- State: Florida
- Zip Code: 34613
- Country Name: United States
- Address: 12395 Cortez Blvd, Brooksville, Florida 34613, United States
- Country: United States

## Related Documents

- FDA Inspection 1304562 - LifeSouth Community Blood Centers, Inc. - 2026-02-24 — source: FDA, date: February 24, 2026
- FDA Inspection 1304562 - LifeSouth Community Blood Centers, Inc. - 2026-02-24 — classification: No Action Indicated (NAI), source: FDA, date: February 24, 2026
- FDA Inspection 1159807 - LifeSouth Community Blood Centers, Inc. - 2021-12-08 — classification: No Action Indicated (NAI), source: FDA, date: December 8, 2021
- FDA Inspection 1159807 - LifeSouth Community Blood Centers, Inc. - 2021-12-08 — classification: No Action Indicated (NAI), source: FDA, date: December 8, 2021
- FDA Inspection 1054560 - LifeSouth Community Blood Centers, Inc. - 2018-05-07 — classification: No Action Indicated (NAI), source: FDA, date: May 7, 2018
- FDA Inspection 987323 - LifeSouth Community Blood Centers, Inc. - 2016-05-11 — classification: No Action Indicated (NAI), source: FDA, date: May 11, 2016
- FDA Inspection 888845 - LifeSouth Community Blood Centers, Inc. - 2014-07-15 — classification: No Action Indicated (NAI), source: FDA, date: July 15, 2014
- FDA Inspection 792384 - LifeSouth Community Blood Centers, Inc. - 2012-07-26 — classification: No Action Indicated (NAI), source: FDA, date: July 26, 2012
- FDA Inspection 666059 - LifeSouth Community Blood Centers, Inc. - 2010-06-10 — classification: No Action Indicated (NAI), source: FDA, date: June 10, 2010

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