# La Jolla IVF - Inspection Records

Source: https://www.keypedia.com/companies/la-jolla-ivf/9da28f0e-d070-44ce-a120-851239712aff

> Inspection records and compliance data for La Jolla IVF in La Jolla, California. Access full analysis and detailed observations.

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## Details

- Name: La Jolla IVF
- FEI Number: 3003942498
- City: La Jolla
- State: California
- Country Name: United States
- Address Line 1: 9850 Genesee Ave Ste 610
- Zip Code: 92037

## Related Documents

- [FDA Inspection 1315918 - La Jolla IVF - 2026-04-23](https://www.keypedia.com/records/fda_inspections/la-jolla-ivf/c1a6b141-ee61-4d81-9bcc-8715e02b1b9f) — classification: No Action Indicated (NAI), source: FDA, date: April 23, 2026
- [FDA Inspection 1216984 - La Jolla IVF - 2023-08-07](https://www.keypedia.com/records/fda_inspections/la-jolla-ivf/2802c5c7-351a-48ae-82c1-0edabd021d5b) — classification: No Action Indicated (NAI), source: FDA, date: August 7, 2023
- [FDA Inspection 1216984 - La Jolla IVF - 2023-08-07](https://www.keypedia.com/records/fda_inspections/la-jolla-ivf/23509bf7-794d-43e2-9a96-153f1e2ed196) — classification: No Action Indicated (NAI), source: FDA, date: August 7, 2023
- [FDA Inspection 1059998 - La Jolla IVF - 2018-07-13](https://www.keypedia.com/records/fda_inspections/la-jolla-ivf/7ea5a89b-40bc-4b32-93ff-6c37d9ae14e6) — classification: No Action Indicated (NAI), source: FDA, date: July 13, 2018
- [FDA Inspection 1059998 - La Jolla IVF - 2018-07-13](https://www.keypedia.com/records/fda_inspections/la-jolla-ivf/decb3bfb-d7bb-45bd-87f6-15c8282df6b5) — classification: No Action Indicated (NAI), source: FDA, date: July 13, 2018
- [FDA Inspection 911460 - La Jolla IVF - 2015-01-22](https://www.keypedia.com/records/fda_inspections/la-jolla-ivf/ad4793e5-793e-42f1-85db-594706991897) — classification: No Action Indicated (NAI), source: FDA, date: January 22, 2015
- [FDA Inspection 680725 - La Jolla IVF - 2010-09-17](https://www.keypedia.com/records/fda_inspections/la-jolla-ivf/ab62f414-194d-4722-b267-b8f36be9c864) — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 17, 2010

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