# The American National Red Cross, Tucson, AZ – FDA Inspections

Source: https://www.keypedia.com/companies/the-american-national-red-cross/154a2acc-4b18-4586-8432-ddaa4aec8322

> Inspection records and compliance data for The American National Red Cross in Tucson, Arizona. 8 FDA inspections on record, last inspected December 08, 2023.

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## Details

- Name: The American National Red Cross
- FEI Number: 2072997
- Address Line 1: 3470 E Universal Way
- City: Tucson
- State: Arizona
- Zip Code: 85756
- Country Name: United States
- Address: 3470 E Universal Way, Tucson, Arizona 85756, United States
- Country: United States

## Related Documents

- [FDA Inspection 1226479 - The American National Red Cross - 2023-12-08](https://www.keypedia.com/records/fda_inspections/the-american-national-red-cross/fc2b3221-ca94-406d-9628-3aa43dceacf4) — classification: No Action Indicated (NAI), source: FDA, date: December 8, 2023
- FDA Inspection 1081461 - The American National Red Cross - 2019-01-25 — classification: No Action Indicated (NAI), source: FDA, date: January 25, 2019
- FDA Inspection 1020977 - The American National Red Cross - 2017-07-12 — classification: No Action Indicated (NAI), source: FDA, date: July 12, 2017
- FDA Inspection 942492 - The American National Red Cross - 2015-09-15 — classification: No Action Indicated (NAI), source: FDA, date: September 15, 2015
- FDA Inspection 829647 - The American National Red Cross - 2013-04-25 — classification: No Action Indicated (NAI), source: FDA, date: April 25, 2013
- FDA Inspection 747025 - The American National Red Cross - 2011-09-23 — classification: No Action Indicated (NAI), source: FDA, date: September 23, 2011
- FDA Inspection 682870 - The American National Red Cross - 2010-09-10 — classification: No Action Indicated (NAI), source: FDA, date: September 10, 2010
- [FDA Inspection 615129 - The American National Red Cross - 2009-09-23](https://www.keypedia.com/records/fda_inspections/the-american-national-red-cross/c4dae80d-424c-4a32-9985-f4680b62d494) — classification: No Action Indicated (NAI), source: FDA, date: September 23, 2009

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