# Electrolux Professional S.p.A. – FDA Inspection, May 8, 2025

Source: https://www.keypedia.com/records/fda_inspections/electrolux-professional-spa/0fa008d9-9699-4388-85ff-7a1cd00498cf
Source feed: FDA_Inspections

> FDA inspection 1269854 of Electrolux Professional S.p.A., May 08, 2025. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR parts 1010 and 1030. Form 483 issued.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1269854
- Company Name: Electrolux Professional S.p.A.
- Inspection Date: 2025-05-08
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Radiation Control and Health Safety Act (RCHSA) Authority
- Product Type: Medical Devices & Rad Health
- Center: Medical Devices & Rad Health
- Office Name: Office of Inspections and Investigations
- Citation Count: 2

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/fouad-attioui/640028ab-0cdd-43c8-816f-433f19c7ad3d)
- Issuing Officer

Company: https://www.keypedia.com/companies/electrolux-professional-spa/14baf593-2b6c-4f08-a982-c37183b76b93

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