# LifeServe Blood Center, Marshalltown, IA – FDA Inspections

Source: https://www.keypedia.com/companies/lifeserve-blood-center/36571368-e55f-4cae-8157-55a511e8bbbd

> Inspection records and compliance data for LifeServe Blood Center in Marshalltown, Iowa. 8 FDA inspections on record, last inspected September 03, 2025.

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## Details

- Name: LifeServe Blood Center
- FEI Number: 3003294564
- Address Line 1: 3109 S Center St Ste 104
- City: Marshalltown
- State: Iowa
- Zip Code: 50158
- Country Name: United States
- Address: 3109 S Center St Ste 104, Marshalltown, Iowa 50158, United States
- Country: United States

## Related Documents

- FDA Inspection 1284328 - LifeServe Blood Center - 2025-09-03 — source: FDA, date: September 3, 2025
- FDA Inspection 1284328 - LifeServe Blood Center - 2025-09-03 — classification: No Action Indicated (NAI), source: FDA, date: September 3, 2025
- FDA Inspection 1206305 - LifeServe Blood Center - 2023-04-19 — classification: No Action Indicated (NAI), source: FDA, date: April 19, 2023
- FDA Inspection 1072981 - LifeServe Blood Center - 2018-10-23 — classification: No Action Indicated (NAI), source: FDA, date: October 23, 2018
- FDA Inspection 1000915 - LifeServe Blood Center - 2017-01-30 — classification: No Action Indicated (NAI), source: FDA, date: January 30, 2017
- [FDA Inspection 915444 - LifeServe Blood Center - 2015-02-18](https://www.keypedia.com/records/fda_inspections/lifeserve-blood-center/b0bbecc6-560e-4c74-8a92-db2984dbaf8a) — classification: Voluntary Action Indicated (VAI), source: FDA, date: February 18, 2015
- FDA Inspection 818532 - LifeServe Blood Center - 2013-02-12 — classification: No Action Indicated (NAI), source: FDA, date: February 12, 2013
- FDA Inspection 698890 - LifeServe Blood Center - 2010-11-23 — classification: No Action Indicated (NAI), source: FDA, date: November 23, 2010
- [FDA Inspection 544413 - LifeServe Blood Center - 2008-10-29](https://www.keypedia.com/records/fda_inspections/lifeserve-blood-center/b03e88ec-4466-42e3-aa84-41c19a187fa1) — classification: No Action Indicated (NAI), source: FDA, date: October 29, 2008

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