# FDA Inspection 1278218 - EUROMI S.A. - July 31, 2025

Source: https://www.keypedia.com/records/fda_inspections/euromi-sa/b2ca4486-ce8a-45fb-bc25-1e1034f1af2c
Source feed: FDA_Inspections

> FDA Inspection 1278218 for EUROMI S.A. on July 31, 2025. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1278218
- Company Name: EUROMI S.A.
- Inspection Date: 2025-07-31
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Medical Devices
- Product Type: Medical Devices & Rad Health
- Office Name: Office of Inspections and Investigations

## Related Documents

- [FDA Inspection 1278218 - 2025-07-31](https://www.keypedia.com/records/fda_inspections/euromi-sa/49a23888-e709-44ec-948f-b863f7e79346)
- [FDA Inspection 1278218 - 2025-07-31](https://www.keypedia.com/records/fda_inspections/euromi-sa/7b165661-1030-4555-b551-2b6b47f0d290)
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Company: https://www.keypedia.com/companies/euromi-sa/117d63e2-e079-4816-8804-517c2fde2bf6

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