# Blood Assurance Inc., Hixson, TN – FDA Inspections

Source: https://www.keypedia.com/companies/blood-assurance-inc/a24f6a50-b83c-4267-98ae-b9b3e6c7d686

> Inspection records and compliance data for Blood Assurance Inc. in Hixson, Tennessee. 8 FDA inspections on record, 1 Form 483, last inspected December 20, 2024.

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## Details

- Name: Blood Assurance Inc.
- FEI Number: 3002660779
- Address Line 1: 1920 Northpoint Blvd
- City: Hixson
- State: Tennessee
- Zip Code: 37343
- Country Name: United States
- Address: 1920 Northpoint Blvd, Hixson, Tennessee 37343, United States
- Country: United States

## Related Documents

- FDA Inspection 1259198 - Blood Assurance Inc. - 2024-12-20 — source: FDA, date: December 20, 2024
- FDA Inspection 1259198 - Blood Assurance Inc. - 2024-12-20 — classification: No Action Indicated (NAI), source: FDA, date: December 20, 2024
- [FDA Inspection 1115271 - Blood Assurance Inc. - 2020-01-17](https://www.keypedia.com/records/fda_inspections/blood-assurance-inc/4a789648-5b54-43ee-b4a6-2fdb67e8f0c3) — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 17, 2020
- [FDA Inspection 1035323 - Blood Assurance Inc. - 2017-12-19](https://www.keypedia.com/records/fda_inspections/blood-assurance-inc/9cb71365-2c85-438e-84be-e079060b6cbb) — classification: Voluntary Action Indicated (VAI), source: FDA, date: December 19, 2017
- FDA Inspection 948599 - Blood Assurance Inc. - 2015-11-04 — classification: No Action Indicated (NAI), source: FDA, date: November 4, 2015
- FDA Inspection 872946 - Blood Assurance Inc. - 2014-03-19 — classification: No Action Indicated (NAI), source: FDA, date: March 19, 2014
- FDA Inspection 811619 - Blood Assurance Inc. - 2012-12-21 — classification: No Action Indicated (NAI), source: FDA, date: December 21, 2012
- FDA Inspection 714287 - Blood Assurance Inc. - 2011-03-03 — classification: No Action Indicated (NAI), source: FDA, date: March 3, 2011
- FDA Inspection 568136 - Blood Assurance Inc. - 2009-02-24 — classification: No Action Indicated (NAI), source: FDA, date: February 24, 2009

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