# Cortex Manufacturing Inc. – FDA Inspection, Sep 19, 2024

Source: https://www.keypedia.com/records/fda_inspections/cortex-manufacturing-inc/b585194b-ad9b-430a-a78c-becb35dcc42f
Source feed: FDA_Inspections

> FDA inspection 1249659 of Cortex Manufacturing Inc., September 19, 2024. Classification: Voluntary Action Indicated (VAI). 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: 1249659
- Company Name: Cortex Manufacturing Inc.
- Inspection Date: 2024-09-19
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Medical Devices
- Product Type: Medical Devices & Rad Health
- Center: Medical Devices & Rad Health
- Office Name: New Orleans District Office
- Citation Count: 1

## Related Documents

- [FDA Inspection 1038630 - 2018-01-25](https://www.keypedia.com/records/fda_inspections/cortex-manufacturing-inc/c40a0721-d2eb-4350-b4b7-caf820909af7)
- [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/nikki-s-bryant/fe859d4f-23a6-4bc9-94c6-5b3c3fe8d99a)

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

Office: https://www.keypedia.com/offices/new-orleans-district-office/95352142-b992-4e06-849d-d7483c0959ea