# Huntington Reproductive Center, Encino, CA – FDA Inspections

Source: https://www.keypedia.com/companies/huntington-reproductive-center/3f833d14-a6b4-424b-8dc5-30f8759ab934

> Inspection records and compliance data for Huntington Reproductive Center in Encino, California. 6 FDA inspections on record, last inspected September 15, 2025.

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## Details

- Name: Huntington Reproductive Center
- FEI Number: 3006501093
- Address Line 1: 15503 Ventura Blvd Ste 200
- City: Encino
- State: California
- Zip Code: 91436
- Country Name: United States
- Address: 15503 Ventura Blvd Ste 200, Encino, California 91436, United States
- Country: United States

## Related Documents

- FDA Inspection 1293834 - Huntington Reproductive Center - 2025-09-15 — classification: No Action Indicated (NAI), source: FDA, date: September 15, 2025
- FDA Inspection 1264971 - Huntington Reproductive Center - 2025-03-19 — source: FDA, date: March 19, 2025
- FDA Inspection 1264971 - Huntington Reproductive Center - 2025-03-19 — classification: No Action Indicated (NAI), source: FDA, date: March 19, 2025
- FDA Inspection 1086929 - Huntington Reproductive Center - 2019-03-29 — classification: No Action Indicated (NAI), source: FDA, date: March 29, 2019
- FDA Inspection 1086929 - Huntington Reproductive Center - 2019-03-29 — classification: No Action Indicated (NAI), source: FDA, date: March 29, 2019
- FDA Inspection 866901 - Huntington Reproductive Center - 2014-02-12 — classification: No Action Indicated (NAI), source: FDA, date: February 12, 2014
- [FDA Inspection 739237 - Huntington Reproductive Center - 2011-08-11](https://www.keypedia.com/records/fda_inspections/huntington-reproductive-center/9c0f4dfb-967d-4437-b268-6433cc8e9d49) — classification: Voluntary Action Indicated (VAI), source: FDA, date: August 11, 2011
- [FDA Inspection 599961 - Huntington Reproductive Center - 2009-07-09](https://www.keypedia.com/records/fda_inspections/huntington-reproductive-center/4d486c2e-4a59-4211-9e4e-c96308de0c5f) — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 9, 2009

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