# FDA 483 - VIOS - February 03, 2107

Source: https://www.globalkeysolutions.net/records/483/vios/5ef554b3-5f6f-468f-a5b6-dc8f26d6d47d

> FDA 483 for VIOS on February 03, 2107. Product: biologics. Access full analysis and detailed observations.

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## Details

- Record Type: 483
- Company Name: VIOS
- Inspection Date: 2107-02-03
- Product Type: biologics
- Office Name: Chicago District Office
- Summary: An FDA inspection of Center For Reproductive Health/Joliet IVF LLC in Crest Hill, Illinois, revealed significant deficiencies in their human reproductive tissue operations. The firm failed to properly determine and document oocyte donor eligibility, including incomplete physical assessments and medical history interviews. Additionally, donor eligibility records were found to be inaccurate, with altered and conflicting dates, and the firm did not follow its own procedures for screening donors for infection.

## Related Officers

- [Debra L. Boyd-Seale](https://www.globalkeysolutions.net/people/debra-l-boyd-seale/6f9af6f9-8deb-494d-b73e-fca63b95d7d2)

Company: https://www.globalkeysolutions.net/companies/vios/3f38b5bd-e864-41f3-bab4-4bc49186283f

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