# Cortex Manufacturing Inc. – FDA Inspection, Jan 25, 2018

Source: https://www.keypedia.com/records/fda_inspections/cortex-manufacturing-inc/c40a0721-d2eb-4350-b4b7-caf820909af7
Source feed: FDA_Inspections

> FDA inspection 1038630 of Cortex Manufacturing Inc., January 25, 2018. Classification: No Action Indicated (NAI). 1 citation under 21 CFR part 820. Form 483 issued. 4 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1038630
- Company Name: Cortex Manufacturing Inc.
- Inspection Date: 2018-01-25
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 1

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- [FDA Inspection 923054 - 2015-04-01](https://www.keypedia.com/records/fda_inspections/cortex-manufacturing-inc/58fa5640-a3b2-4f4f-9921-c480e2da91de)
- [FDA Inspection 814187 - 2013-01-15](https://www.keypedia.com/records/fda_inspections/cortex-manufacturing-inc/c307a8dc-5170-419c-9c26-9f41db423e5f)
- FDA Inspection 727209 - 2011-05-23

## Related Officers

- [Company Rep](https://www.keypedia.com/people/paul-m-kawamoto/0a24b110-12de-4736-8d98-7a023ceec01e)

Company: https://www.keypedia.com/companies/cortex-manufacturing-inc/6a8cda79-2855-47c5-b63b-4b78678508fa

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7