# UC San Diego Health Clinical Lab - Hillcrest, San Diego, CA – FDA Inspections

Source: https://www.keypedia.com/companies/uc-san-diego-health-clinical-lab-hillcrest/b2ef32f3-6a0e-4ee9-b700-b73228e002c5

> Inspection records and compliance data for UC San Diego Health Clinical Lab - Hillcrest in San Diego, California. 6 FDA inspections on record, last inspected October 29, 2024.

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## Details

- Name: UC San Diego Health Clinical Lab - Hillcrest
- FEI Number: 2071483
- Address Line 1: 200 W Arbor Dr
- City: San Diego
- State: California
- Zip Code: 92103
- Country Name: United States
- Address: 200 W Arbor Dr, San Diego, California 92103, United States
- Country: United States

## Related Documents

- FDA Inspection 1255961 - UC San Diego Health Clinical Lab - Hillcrest - 2024-10-29 — source: FDA, date: October 29, 2024
- FDA Inspection 1255961 - UC San Diego Health Clinical Lab - Hillcrest - 2024-10-29 — classification: No Action Indicated (NAI), source: FDA, date: October 29, 2024
- FDA Inspection 1100244 - UC San Diego Health Clinical Lab - Hillcrest - 2019-07-26 — classification: No Action Indicated (NAI), source: FDA, date: July 26, 2019
- FDA Inspection 1015624 - UC San Diego Health Clinical Lab - Hillcrest - 2017-06-08 — classification: No Action Indicated (NAI), source: FDA, date: June 8, 2017
- FDA Inspection 943778 - UC San Diego Health Clinical Lab - Hillcrest - 2015-08-20 — classification: No Action Indicated (NAI), source: FDA, date: August 20, 2015
- [FDA Inspection 812462 - UC San Diego Health Clinical Lab - Hillcrest - 2012-12-31](https://www.keypedia.com/records/fda_inspections/uc-san-diego-health-clinical-lab-hillcrest/f712bfde-ced4-4ea6-b68c-b2e6449641fc) — classification: Voluntary Action Indicated (VAI), source: FDA, date: December 31, 2012
- [FDA Inspection 733782 - UC San Diego Health Clinical Lab - Hillcrest - 2011-07-08](https://www.keypedia.com/records/fda_inspections/uc-san-diego-health-clinical-lab-hillcrest/72c7cfb6-7be6-4289-a0b2-52a5dec99d04) — classification: No Action Indicated (NAI), source: FDA, date: July 8, 2011

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