# FDA 483 - Xttrium Laboratories, Inc. - December 03, 2024

Source: https://www.keypedia.com/records/483/xttrium-laboratories-inc/f27a0c35-886c-4e51-a07d-155b8f0623b6

> FDA 483 for Xttrium Laboratories, Inc. on December 03, 2024. Product: drugs. Access full analysis and detailed observations.

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## Details

- Record Type: 483
- Company Name: Xttrium Laboratories, Inc.
- Inspection Date: 2024-12-03
- Product Type: drugs
- Office Name: Chicago District Office
- Summary: Xitrium Laboratories, Inc. in Lake Villa, IL, an API manufacturer, was cited for significant deficiencies across multiple areas of its quality system. Observations included failures in drug substance stability testing, inadequate sampling plans for process validation, and insufficient cleaning validation. Additionally, poor deviation management and issues with equipment cleaning procedures and construction were noted, posing risks to API quality.

## Related Officers

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Company: https://www.keypedia.com/companies/xttrium-laboratories-inc/d7da0137-e482-4f12-ad9e-02fa6b48daad

Office: https://www.keypedia.com/offices/chicago-district-office/a510300b-0eaf-4a33-90b5-231d95977669
