# FDA Inspection 1275975 - VRL Eurofins - July 18, 2025

Source: https://www.keypedia.com/records/fda_inspections/vrl-eurofins/d4571d2c-b6bb-4d42-ab45-cc4c61b4ea2e
Source feed: FDA_Inspections

> FDA Inspection 1275975 for VRL Eurofins on July 18, 2025. Classification: Voluntary Action Indicated (VAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1275975
- Company Name: VRL Eurofins
- Inspection Date: 2025-07-18
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Human Cellular, Tissue, and Gene Therapies
- Product Type: Biologics
- Office Name: San Francisco District Office

## Related Documents

- [FDA Inspection 1148670 - 2021-08-02](https://www.keypedia.com/records/fda_inspections/vrl-eurofins/746706d3-4c79-434f-97b7-25cde7923695)
- [FDA Inspection 1148670 - 2021-08-02](https://www.keypedia.com/records/fda_inspections/vrl-eurofins/1918fd00-fac3-4572-a9dd-72bf5ba5b6b2)

Company: https://www.keypedia.com/companies/vrl-eurofins/1fe12b61-5415-466b-b400-66bd6cfa8de7

Office: https://www.keypedia.com/offices/san-francisco-district-office/6f838e9c-aae1-4665-9c46-a51d43be02df