# Huntington Reproductive Center Medical Group dba HRC Fertility, Westlake Village, CA – FDA Inspections

Source: https://www.keypedia.com/companies/huntington-reproductive-center-medical-group-dba-hrc-fertility/d828184e-40f6-4914-ae79-17edaeaf8158

> Inspection records and compliance data for Huntington Reproductive Center Medical Group dba HRC Fertility in Westlake Village, California. 4 FDA inspections on record, 1 Form 483, last inspected April 26, 2018.

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## Details

- Name: Huntington Reproductive Center Medical Group dba HRC Fertility
- FEI Number: 3005108085
- Address Line 1: 1220 La Venta Dr Ste 103
- City: Westlake Village
- State: California
- Zip Code: 91361
- Country Name: United States
- Address: 1220 La Venta Dr Ste 103, Westlake Village, California 91361, United States
- Country: United States

## Related Documents

- [FDA Inspection 1049830 - Huntington Reproductive Center Medical Group dba HRC Fertility - 2018-04-26](https://www.keypedia.com/records/fda_inspections/huntington-reproductive-center-medical-group-dba-hrc-fertility/b0c6d0e9-a09c-45c1-82c4-ebf990636669) — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 26, 2018
- FDA Inspection 1049830 - Huntington Reproductive Center Medical Group dba HRC Fertility - 2018-04-26 — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 26, 2018
- [FDA Inspection 920649 - Huntington Reproductive Center Medical Group dba HRC Fertility - 2015-02-05](https://www.keypedia.com/records/fda_inspections/huntington-reproductive-center-medical-group-dba-hrc-fertility/b16af774-e3e1-4ce8-9e95-1e7cf2c4f692) — classification: Voluntary Action Indicated (VAI), source: FDA, date: February 5, 2015
- FDA Inspection 761103 - Huntington Reproductive Center Medical Group dba HRC Fertility - 2011-12-22 — classification: No Action Indicated (NAI), source: FDA, date: December 22, 2011
- FDA Inspection 679893 - Huntington Reproductive Center Medical Group dba HRC Fertility - 2010-09-10 — classification: No Action Indicated (NAI), source: FDA, date: September 10, 2010

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