# FDA 483 - Viera Fertility Center - February 03, 2023

Source: https://www.keypedia.com/records/483/viera-fertility-center/714d443f-fdbe-4c7b-92de-9abb8c12ec10

> FDA 483 for Viera Fertility Center on February 03, 2023. Product: other. Access full analysis and detailed observations.

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## Details

- Record Type: 483
- Company Name: Viera Fertility Center
- Inspection Date: 2023-02-03
- Product Type: other
- Office Name: Office of Medical Device and Radiological Health Division II
- Summary: An FDA inspection of Viera Fertility Center in Melbourne, FL, identified a significant issue regarding donor screening practices. The firm failed to adequately screen donors for risk factors of communicable disease agents, specifically concerning Zika virus (ZIKV) transmission. This indicates a potential risk in their reproductive establishment operations.

## Related Documents

- [483 - 2019-06-05](https://www.keypedia.com/records/483/viera-fertility-center/950d1377-077b-4d27-aca4-0966fa9ac4f2)

## Related Officers

- [Lura Baquero](https://www.keypedia.com/people/lura-baquero/55dc6eb5-01d5-427e-a3ef-cc6ca35f3837)

Company: https://www.keypedia.com/companies/viera-fertility-center/25b4c965-5aa9-48d7-803f-c9575927063b

Office: https://www.keypedia.com/offices/office-of-medical-device-and-radiological-health-division-ii/ae9bd439-479a-420d-9dd8-9fe1fc0863d6