# FDA Inspection 1283776 - EUROSIREL S.P.A - September 26, 2025

Source: https://www.keypedia.com/records/fda_inspections/eurosirel-spa/8500073a-8809-4b35-b9b3-a02c43889bc5
Source feed: FDA_Inspections

> FDA Inspection 1283776 for EUROSIREL S.P.A on September 26, 2025. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1283776
- Company Name: EUROSIREL S.P.A
- Inspection Date: 2025-09-26
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Drug Quality Assurance
- Product Type: Human Drugs
- Office Name: Office of Inspections and Investigations

## Related Documents

- [FDA Inspection 1243970 - 2024-05-24](https://www.keypedia.com/records/fda_inspections/eurosirel-spa/9e144865-1692-4134-87c4-c2f5fb818b52)

Company: https://www.keypedia.com/companies/eurosirel-spa/16e9f1c9-4890-46e2-a5fc-155ab2bd65fa

Office: https://www.keypedia.com/offices/office-of-inspections-and-investigations/7dd0b904-a3df-46bc-a7b2-70ddb6f809c8