# Cortex Manufacturing Inc. – FDA Inspection, Jan 15, 2013

Source: https://www.keypedia.com/records/fda_inspections/cortex-manufacturing-inc/c307a8dc-5170-419c-9c26-9f41db423e5f
Source feed: FDA_Inspections

> FDA inspection 814187 of Cortex Manufacturing Inc., January 15, 2013. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. 4 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 814187
- Company Name: Cortex Manufacturing Inc.
- Inspection Date: 2013-01-15
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 2

## Related Documents

- [FDA Inspection 1249659 - 2024-09-19](https://www.keypedia.com/records/fda_inspections/cortex-manufacturing-inc/b585194b-ad9b-430a-a78c-becb35dcc42f)
- [FDA Inspection 1038630 - 2018-01-25](https://www.keypedia.com/records/fda_inspections/cortex-manufacturing-inc/c40a0721-d2eb-4350-b4b7-caf820909af7)
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- FDA Inspection 727209 - 2011-05-23

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