# San Diego Blood Bank, San Diego, CA – FDA Inspections

Source: https://www.keypedia.com/companies/san-diego-blood-bank/060fd935-0b88-4d98-95b3-ff4ebb1a1a7f

> Inspection records and compliance data for San Diego Blood Bank in San Diego, California. 7 FDA inspections on record, last inspected February 24, 2025.

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## Details

- Name: San Diego Blood Bank
- FEI Number: 2075359
- Address Line 1: 3636 Gateway Center Ave Ste 100
- City: San Diego
- State: California
- Zip Code: 92102
- Country Name: United States
- Address: 3636 Gateway Center Ave Ste 100, San Diego, California 92102, United States
- Country: United States

## Related Documents

- FDA Inspection 1263923 - San Diego Blood Bank - 2025-02-24 — source: FDA, date: February 24, 2025
- FDA Inspection 1263923 - San Diego Blood Bank - 2025-02-24 — classification: No Action Indicated (NAI), source: FDA, date: February 24, 2025
- FDA Inspection 1148693 - San Diego Blood Bank - 2021-08-05 — classification: No Action Indicated (NAI), source: FDA, date: August 5, 2021
- FDA Inspection 1148693 - San Diego Blood Bank - 2021-08-05 — classification: No Action Indicated (NAI), source: FDA, date: August 5, 2021
- FDA Inspection 1066189 - San Diego Blood Bank - 2018-08-28 — classification: No Action Indicated (NAI), source: FDA, date: August 28, 2018
- FDA Inspection 970190 - San Diego Blood Bank - 2016-03-31 — classification: No Action Indicated (NAI), source: FDA, date: March 31, 2016
- [FDA Inspection 840220 - San Diego Blood Bank - 2013-07-12](https://www.keypedia.com/records/fda_inspections/san-diego-blood-bank/e1916a7c-aa02-47da-b148-30678dd88855) — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 12, 2013
- [FDA Inspection 743860 - San Diego Blood Bank - 2011-09-13](https://www.keypedia.com/records/fda_inspections/san-diego-blood-bank/75836e8e-bef2-49c8-98f4-3a26ff7ca5a1) — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 13, 2011
- FDA Inspection 591323 - San Diego Blood Bank - 2009-06-23 — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 23, 2009

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