# FDA 483 - Essex Industries, Inc. - February 23, 2026

Source: https://www.keypedia.com/records/483/essex-industries-inc/51782313-e107-4e4c-9c74-670b198972c6

> FDA 483 for Essex Industries, Inc. on February 23, 2026. Product: device. Access full analysis and detailed observations.

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## Details

- Record Type: 483
- Company Name: Essex Industries, Inc.
- Inspection Date: 2026-02-23
- Product Type: device
- Office Name: Kansas City District Office
- Summary: An FDA inspection of Essex Industries, Inc. in Affton, MO, from February 18-23, 2026, identified a significant compliance issue. The firm failed to submit required Unique Device Identification (UDI) information to the Global Unique Device Identification Database (GUDID) for its commercially distributed medical devices. This indicates a lapse in regulatory reporting for device identification.

## Related Documents

- [483 - 2022-12-16](https://www.keypedia.com/records/483/essex-industries-inc/ea009394-1224-41e8-83f7-563684cddbed)

## Related Officers

- [Edward E. Lockwood](https://www.keypedia.com/people/edward-e-lockwood/3260b39e-9211-489f-8247-0ec3353e57ca)

Company: https://www.keypedia.com/companies/essex-industries-inc/ea0b5450-4e1e-41b1-aaf5-57c27d5f2521

Office: https://www.keypedia.com/offices/kansas-city-district-office/cd397ab1-df4e-46f1-ab1c-0f6db9abcf79