# FDA Inspection 1038630 - Cortex Manufacturing Inc. - January 25, 2018

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

> FDA Inspection 1038630 for Cortex Manufacturing Inc. on January 25, 2018. Classification: No Action Indicated (NAI).

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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)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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

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