# LifeServe Blood Center - Inspection Records

Source: https://www.globalkeysolutions.net/companies/lifeserve-blood-center/875acc80-dad7-42e4-a8a5-b700667241d9

> Inspection records and compliance data for LifeServe Blood Center in Mitchell, South Dakota. Access full analysis and detailed observations.

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## Details

- Name: LifeServe Blood Center
- FEI Number: 3006192368
- City: Mitchell
- State: South Dakota
- Country Name: United States
- Address Line 1: 8419 E Spruce St, Suite 150
- Zip Code: 57301

## Related Documents

- [FDA Inspection 1103051 - LifeServe Blood Center - 2019-09-27](https://www.globalkeysolutions.net/records/fda_inspections/lifeserve-blood-center/6d49bcf2-f5a0-43a2-97b8-376d68460b60) — classification: No Action Indicated (NAI), source: FDA, date: September 27, 2019
- [FDA Inspection 1019656 - LifeServe Blood Center - 2017-06-26](https://www.globalkeysolutions.net/records/fda_inspections/lifeserve-blood-center/9acb1bd8-9ee6-4946-86b1-261d3a3ec449) — classification: No Action Indicated (NAI), source: FDA, date: June 26, 2017
- [FDA Inspection 905259 - LifeServe Blood Center - 2014-11-07](https://www.globalkeysolutions.net/records/fda_inspections/lifeserve-blood-center/d9aa3120-7926-404f-bfe0-d4da18866b17) — classification: No Action Indicated (NAI), source: FDA, date: November 7, 2014
- [FDA Inspection 810901 - LifeServe Blood Center - 2012-11-28](https://www.globalkeysolutions.net/records/fda_inspections/lifeserve-blood-center/3e215213-834c-4ea1-a9ab-b89197b66a29) — classification: No Action Indicated (NAI), source: FDA, date: November 28, 2012
- [FDA Inspection 707678 - LifeServe Blood Center - 2011-01-26](https://www.globalkeysolutions.net/records/fda_inspections/lifeserve-blood-center/fe92bdb3-e858-4553-8683-c9badf6148ef) — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 26, 2011
- [FDA Inspection 681384 - LifeServe Blood Center - 2010-07-28](https://www.globalkeysolutions.net/records/fda_inspections/lifeserve-blood-center/b638dd53-3011-41ce-9078-004c82a4bcac) — classification: No Action Indicated (NAI), source: FDA, date: July 28, 2010

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