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

Source: https://www.keypedia.com/companies/san-diego-eye-bank/d6ec2baa-532b-4559-b23b-fde1f35ce16e

> Inspection records and compliance data for San Diego Eye Bank in San Diego, California. 6 FDA inspections on record, last inspected May 03, 2024.

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## Details

- Name: San Diego Eye Bank
- FEI Number: 3002515992
- Address Line 1: 3870 Murphy Canyon Rd Ste 250
- City: San Diego
- State: California
- Zip Code: 92123
- Country Name: United States
- Address: 3870 Murphy Canyon Rd Ste 250, San Diego, California 92123, United States
- Country: United States

## Related Documents

- [FDA Inspection 1237570 - San Diego Eye Bank - 2024-05-03](https://www.keypedia.com/records/fda_inspections/san-diego-eye-bank/f5c986c3-02f4-4ae3-b165-6cffbe2c5a81) — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 3, 2024
- FDA Inspection 1237570 - San Diego Eye Bank - 2024-05-03 — classification: No Action Indicated (NAI), source: FDA, date: May 3, 2024
- FDA Inspection 1032340 - San Diego Eye Bank - 2017-11-03 — classification: No Action Indicated (NAI), source: FDA, date: November 3, 2017
- FDA Inspection 1032340 - San Diego Eye Bank - 2017-11-03 — classification: No Action Indicated (NAI), source: FDA, date: November 3, 2017
- FDA Inspection 929480 - San Diego Eye Bank - 2015-05-29 — classification: No Action Indicated (NAI), source: FDA, date: May 29, 2015
- FDA Inspection 799479 - San Diego Eye Bank - 2012-08-30 — classification: No Action Indicated (NAI), source: FDA, date: August 30, 2012
- [FDA Inspection 672042 - San Diego Eye Bank - 2010-07-21](https://www.keypedia.com/records/fda_inspections/san-diego-eye-bank/4f815b4c-7de7-4e52-a288-c73a019f7684) — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 21, 2010
- [FDA Inspection 611083 - San Diego Eye Bank - 2009-09-08](https://www.keypedia.com/records/fda_inspections/san-diego-eye-bank/ce58b485-be46-467a-be12-80ffd312f256) — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 8, 2009

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