# FDA 483 - Cton Laboratories - July 25, 2025

Source: https://www.keypedia.com/records/483/cton-laboratories/e7d41862-fa3a-4dd4-837a-0c59b280826f

> FDA 483 for Cton Laboratories on July 25, 2025. Product: biologics. Access full analysis and detailed observations.

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## Details

- Record Type: 483
- Company Name: Cton Laboratories
- Inspection Date: 2025-07-25
- Product Type: biologics
- Office Name: Los Angeles District Office
- Summary: CTON Corporation in Torrance, CA, a testing laboratory for HCT/Ps, received a Form 483 with three observations. The inspection revealed significant deficiencies in establishing and maintaining core Current Good Tissue Practice (CGTP) procedures, a lack of an adequate quality program, and insufficient detail in records. These issues indicate a risk of contamination, cross-contamination, and the spread of communicable diseases.

## Related Documents

- [483 - 2025-07-25](https://www.keypedia.com/records/483/cton-laboratories/a65594f9-c765-4583-8fcb-92e865b012eb)

## Related Officers

- [FDA_PERSONNEL](https://www.keypedia.com/people/maurine-fadlalla/519e6e71-a50a-43b5-b41a-2249ec9afdd5)
- [Creighton T. Tuzon](https://www.keypedia.com/people/creighton-t-tuzon/be0d09c0-59f4-48c3-9e3d-a1ceb2587e3e)

Company: https://www.keypedia.com/companies/cton-laboratories/e1602f48-f4a8-43e6-9bb2-9f9d6f1b6ab0

Office: https://www.keypedia.com/offices/los-angeles-district-office/edcf1dfe-596a-43b8-8df4-07d9cd94763b