# Assisted Reproductive Technologies Medical Group Inc, Encino, CA – FDA Inspections

Source: https://www.keypedia.com/companies/assisted-reproductive-technologies-medical-group-inc/356ededc-ed23-497c-ac93-3e7d3afd7bd8

> Inspection records and compliance data for Assisted Reproductive Technologies Medical Group Inc in Encino, California. 5 FDA inspections on record, last inspected May 27, 2026.

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## Details

- Name: Assisted Reproductive Technologies Medical Group Inc
- FEI Number: 3007014169
- Address Line 1: 5353 Balboa Blvd Ste 301
- City: Encino
- State: California
- Zip Code: 91316
- Country Name: United States
- Address: 5353 Balboa Blvd Ste 301, Encino, California 91316, United States
- Country: United States

## Related Documents

- FDA Inspection 1320230 - Assisted Reproductive Technologies Medical Group Inc - 2026-05-27 — classification: No Action Indicated (NAI), source: FDA, date: May 27, 2026
- FDA Inspection 1200418 - Assisted Reproductive Technologies Medical Group Inc - 2023-03-20 — classification: No Action Indicated (NAI), source: FDA, date: March 20, 2023
- FDA Inspection 1200418 - Assisted Reproductive Technologies Medical Group Inc - 2023-03-20 — classification: No Action Indicated (NAI), source: FDA, date: March 20, 2023
- FDA Inspection 1200418 - Assisted Reproductive Technologies Medical Group Inc - 2023-03-20 — classification: No Action Indicated (NAI), source: FDA, date: March 20, 2023
- FDA Inspection 1060618 - Assisted Reproductive Technologies Medical Group Inc - 2018-06-29 — classification: No Action Indicated (NAI), source: FDA, date: June 29, 2018
- FDA Inspection 960529 - Assisted Reproductive Technologies Medical Group Inc - 2016-02-29 — classification: No Action Indicated (NAI), source: FDA, date: February 29, 2016
- [FDA Inspection 739235 - Assisted Reproductive Technologies Medical Group Inc - 2011-08-03](https://www.keypedia.com/records/fda_inspections/assisted-reproductive-technologies-medical-group-inc/8477b02a-7aa5-4019-9ba7-e225f223eb11) — classification: Voluntary Action Indicated (VAI), source: FDA, date: August 3, 2011

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