Euromed SA
FDA import alert and refusal historyMollet Del Valles, SpainFEI 3010111275
As of October 26, 2026, Euromed SA has no FDA import alert listing or import refusal in SupplierRadar's records; its most recent FDA inspection, on March 20, 2018, was classified NAI (No Action Indicated).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- Classified NAI (No Action Indicated)
Every FDA record for Euromed SA
2 records, newest first. Each line links to the FDA page it came from.
Questions about Euromed SA
- Is Euromed SA on an FDA import alert?
- No listing for Euromed SA appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Spain page.
- Has FDA refused shipments from Euromed SA?
- No FDA import refusals for Euromed SA appear in FDA's refusal data since October 2016, as of October 26, 2026.
- When was Euromed SA last inspected by FDA?
- FDA's most recent inspection of Euromed SA with a final classification is dated March 20, 2018 and was classified NAI (No Action Indicated).
- What is Euromed SA's FEI number?
- Euromed SA's FDA Establishment Identifier (FEI) is 3010111275.
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SupplierRadar is not affiliated with the U.S. Food and Drug Administration. Data comes from public FDA records and may contain errors. This is not legal advice; importers remain responsible for their supplier evaluations.