# Diagnostic Automation/Cortez Diagnostics Inc - Inspection Records

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. Access full analysis and detailed observations.

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## Details

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

## Related Documents

- [FDA Inspection 1208883 - Diagnostic Automation/Cortez Diagnostics Inc - 2023-06-14](https://www.keypedia.com/records/fda_inspections/diagnostic-automationcortez-diagnostics-inc/af6c7eb2-6b32-4d0b-b3e8-13206a3087e1) — 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](https://www.keypedia.com/records/fda_inspections/diagnostic-automationcortez-diagnostics-inc/3032c4e5-e155-484b-8021-36b17b5156fd) — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 15, 2021
- [FDA Inspection 1148421 - Diagnostic Automation/Cortez Diagnostics Inc - 2021-07-15](https://www.keypedia.com/records/fda_inspections/diagnostic-automationcortez-diagnostics-inc/b2e09265-ad9b-4d34-bf6a-6cd31fb297b9) — classification: No Action Indicated (NAI), source: FDA, date: July 15, 2021
- [FDA Inspection 1054618 - Diagnostic Automation/Cortez Diagnostics Inc - 2018-04-13](https://www.keypedia.com/records/fda_inspections/diagnostic-automationcortez-diagnostics-inc/9718efc5-8d6a-4f20-9ad4-89f6831dd12e) — classification: No Action Indicated (NAI), source: FDA, date: April 13, 2018
- [FDA Inspection 1054618 - Diagnostic Automation/Cortez Diagnostics Inc - 2018-04-13](https://www.keypedia.com/records/fda_inspections/diagnostic-automationcortez-diagnostics-inc/5a49c44f-1e99-4ff9-88a0-6f15a82d5b7e) — classification: No Action Indicated (NAI), source: FDA, date: April 13, 2018
- [FDA Inspection 937847 - Diagnostic Automation/Cortez Diagnostics Inc - 2015-08-19](https://www.keypedia.com/records/fda_inspections/diagnostic-automationcortez-diagnostics-inc/b7a5829a-22b3-4828-9673-9af734aaacd6) — 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](https://www.keypedia.com/records/fda_inspections/diagnostic-automationcortez-diagnostics-inc/bf70b5d3-a7d6-4c04-b2fd-19cc077eb57e) — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 28, 2010
- [FDA Inspection 663988 - Diagnostic Automation/Cortez Diagnostics Inc - 2010-05-28](https://www.keypedia.com/records/fda_inspections/diagnostic-automationcortez-diagnostics-inc/b2ad17b5-814c-4271-aecf-f9c014cfa43e) — classification: No Action Indicated (NAI), source: FDA, date: May 28, 2010

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