# LifeStart Fertility Center, Agoura Hills, CA – FDA Inspections

Source: https://www.keypedia.com/companies/lifestart-fertility-center/3b2eab88-17a5-4b21-9501-1dd570d9db9e

> Inspection records and compliance data for LifeStart Fertility Center in Agoura Hills, California. 5 FDA inspections on record, 1 Form 483, last inspected April 22, 2026.

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## Details

- Name: LifeStart Fertility Center
- FEI Number: 3005405793
- Address Line 1: 29525 Canwood St Ste 210
- City: Agoura Hills
- State: California
- Zip Code: 91301
- Country Name: United States
- Address: 29525 Canwood St Ste 210, Agoura Hills, California 91301, United States
- Country: United States

## Related Documents

- FDA Inspection 1313634 - LifeStart Fertility Center - 2026-04-22 — classification: No Action Indicated (NAI), source: FDA, date: April 22, 2026
- FDA Inspection 1190223 - LifeStart Fertility Center - 2022-11-07 — classification: No Action Indicated (NAI), source: FDA, date: November 7, 2022
- FDA Inspection 1190223 - LifeStart Fertility Center - 2022-11-07 — classification: No Action Indicated (NAI), source: FDA, date: November 7, 2022
- FDA Inspection 1190223 - LifeStart Fertility Center - 2022-11-07 — classification: No Action Indicated (NAI), source: FDA, date: November 7, 2022
- FDA Inspection 1028858 - LifeStart Fertility Center - 2017-10-06 — classification: Voluntary Action Indicated (VAI), source: FDA, date: October 6, 2017
- [FDA Inspection 1028858 - LifeStart Fertility Center - 2017-10-06](https://www.keypedia.com/records/fda_inspections/lifestart-fertility-center/b2bcca66-fa83-453f-9ffc-2b24067338f2) — classification: Voluntary Action Indicated (VAI), source: FDA, date: October 6, 2017
- [FDA Inspection 920655 - LifeStart Fertility Center - 2015-02-06](https://www.keypedia.com/records/fda_inspections/lifestart-fertility-center/c12d424c-e03d-40bb-b9eb-2b8f95c51d43) — classification: Voluntary Action Indicated (VAI), source: FDA, date: February 6, 2015
- FDA Inspection 742303 - LifeStart Fertility Center - 2011-08-31 — classification: No Action Indicated (NAI), source: FDA, date: August 31, 2011

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