Yurrita & Sons, S.A.
FDA import alert and refusal historyMutriku, SpainFEI 3009974566
As of October 26, 2026, Yurrita & Sons, S.A. has no FDA import alert listing or import refusal in SupplierRadar's records; its most recent FDA inspection, on March 14, 2022, 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 Yurrita & Sons, S.A.
4 records, newest first. Each line links to the FDA page it came from.
2022
- InspectionInspection classified NAI (No Action Indicated)Foodborne Biological HazardsSource
2018
- InspectionInspection classified VAI (Voluntary Action Indicated)Foodborne Biological HazardsSource
2011
- InspectionInspection classified VAI (Voluntary Action Indicated)Foodborne Biological HazardsSource
2010
- InspectionInspection classified VAI (Voluntary Action Indicated)Foodborne Biological HazardsSource
Questions about Yurrita & Sons, S.A.
- Is Yurrita & Sons, S.A. on an FDA import alert?
- No listing for Yurrita & Sons, S.A. 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 Yurrita & Sons, S.A.?
- No FDA import refusals for Yurrita & Sons, S.A. appear in FDA's refusal data since October 2016, as of October 26, 2026.
- When was Yurrita & Sons, S.A. last inspected by FDA?
- FDA's most recent inspection of Yurrita & Sons, S.A. with a final classification is dated March 14, 2022 and was classified NAI (No Action Indicated).
- What is Yurrita & Sons, S.A.'s FEI number?
- Yurrita & Sons, S.A.'s FDA Establishment Identifier (FEI) is 3009974566.
Buying from Yurrita & Sons, S.A.?
Watch it and get the FDA record the day it changes. Free for one supplier.
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.