Queserias del Tietar, S. L.
FDA import alert and refusal historyLa Adrada, SpainFEI 3004292341
As of October 26, 2026, Queserias del Tietar, S. L. has no FDA import alert listing or import refusal in SupplierRadar's records; its most recent FDA inspection, on March 30, 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 Queserias del Tietar, S. L.
3 records, newest first. Each line links to the FDA page it came from.
2022
- InspectionInspection classified NAI (No Action Indicated)Food Composition, Standards, Labeling and Econ; Foodborne Biological HazardsSource
2020
- InspectionInspection classified VAI (Voluntary Action Indicated)Food Composition, Standards, Labeling and Econ; Foodborne Biological HazardsSource
2011
- InspectionInspection classified NAI (No Action Indicated)Food Composition, Standards, Labeling and Econ; Foodborne Biological HazardsSource
Questions about Queserias del Tietar, S. L.
- Is Queserias del Tietar, S. L. on an FDA import alert?
- No listing for Queserias del Tietar, S. L. 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 Queserias del Tietar, S. L.?
- No FDA import refusals for Queserias del Tietar, S. L. appear in FDA's refusal data since October 2016, as of October 26, 2026.
- When was Queserias del Tietar, S. L. last inspected by FDA?
- FDA's most recent inspection of Queserias del Tietar, S. L. with a final classification is dated March 30, 2022 and was classified NAI (No Action Indicated).
- What is Queserias del Tietar, S. L.'s FEI number?
- Queserias del Tietar, S. L.'s FDA Establishment Identifier (FEI) is 3004292341.
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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.