# Diagnostic Automation/Cortez Diagnostics Inc, Woodland Hills, CA – FDA Inspections

Source: https://www.keypedia.com/companies/diagnostic-automationcortez-diagnostics-inc/1780f851-4e22-43ef-818f-eaff1fa4bef1

> Inspection records and compliance data for Diagnostic Automation/Cortez Diagnostics Inc in Woodland Hills, California. 6 FDA inspections on record, last inspected June 14, 2023.

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## Details

- Name: Diagnostic Automation/Cortez Diagnostics Inc
- FEI Number: 1000306617
- Address Line 1: 21250 Califa St Ste 116
- City: Woodland Hills
- State: California
- Zip Code: 91367
- Country Name: United States
- Address: 21250 Califa St Ste 116, Woodland Hills, California 91367, United States
- Country: United States

## Related Documents

- FDA Inspection 1208883 - Diagnostic Automation/Cortez Diagnostics Inc - 2023-06-14 — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 14, 2023
- [483 - Diagnostic Automation/Cortez Diagnostics Inc - 2021-07-15](https://www.keypedia.com/records/483/diagnostic-automationcortez-diagnostics-inc/534524bf-1a8f-4cf3-a02e-b3634d8706d2) — source: FDA, date: July 15, 2021
- FDA Inspection 1148421 - Diagnostic Automation/Cortez Diagnostics Inc - 2021-07-15 — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 15, 2021
- FDA Inspection 1148421 - Diagnostic Automation/Cortez Diagnostics Inc - 2021-07-15 — classification: No Action Indicated (NAI), source: FDA, date: July 15, 2021
- FDA Inspection 1054618 - Diagnostic Automation/Cortez Diagnostics Inc - 2018-04-13 — classification: No Action Indicated (NAI), source: FDA, date: April 13, 2018
- FDA Inspection 1054618 - Diagnostic Automation/Cortez Diagnostics Inc - 2018-04-13 — classification: No Action Indicated (NAI), source: FDA, date: April 13, 2018
- FDA Inspection 937847 - Diagnostic Automation/Cortez Diagnostics Inc - 2015-08-19 — classification: No Action Indicated (NAI), source: FDA, date: August 19, 2015
- [FDA Inspection 803307 - Diagnostic Automation/Cortez Diagnostics Inc - 2012-10-16](https://www.keypedia.com/records/fda_inspections/diagnostic-automationcortez-diagnostics-inc/271e6731-fa1f-4cfe-a5f7-6d9f3bdcdd37) — classification: No Action Indicated (NAI), source: FDA, date: October 16, 2012
- FDA Inspection 663988 - Diagnostic Automation/Cortez Diagnostics Inc - 2010-05-28 — classification: No Action Indicated (NAI), source: FDA, date: May 28, 2010
- FDA Inspection 663988 - Diagnostic Automation/Cortez Diagnostics Inc - 2010-05-28 — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 28, 2010

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