Antonio Garcia Inesta SL
FDA import alert and refusal historyNovelda, SpainFEI 3010145266
As of October 26, 2026, Antonio Garcia Inesta SL is not on any FDA import alert in SupplierRadar's records; FDA refused 3 of its shipment lines between October 4, 2023 and November 6, 2023, most often for filthy, putrid or decomposed substance (FILTHY).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- Saffron, whole (spice) · FILTHY
- Last warning letter
- None found
- Last inspection
- Classified NAI (No Action Indicated)
Every FDA record for Antonio Garcia Inesta SL
4 records, newest first. Each line links to the FDA page it came from.
2023
2018
- InspectionInspection classified NAI (No Action Indicated)Foodborne Biological HazardsSource
Refusal charges, in plain English
Questions about Antonio Garcia Inesta SL
- Is Antonio Garcia Inesta SL on an FDA import alert?
- No listing for Antonio Garcia Inesta SL 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 Antonio Garcia Inesta SL?
- Yes. FDA refused 3 shipment lines from Antonio Garcia Inesta SL between October 4, 2023 and November 6, 2023. The most recent, on November 6, 2023, was saffron, whole (spice), charged as FILTHY (filthy, putrid or decomposed substance).
- Why did FDA refuse Antonio Garcia Inesta SL's shipments?
- The most frequent charges are FILTHY (filthy, putrid or decomposed substance, 3 lines) and OMITTED (omitted, 2 lines).
- When was Antonio Garcia Inesta SL last inspected by FDA?
- FDA's most recent inspection of Antonio Garcia Inesta SL with a final classification is dated June 7, 2018 and was classified NAI (No Action Indicated).
- What is Antonio Garcia Inesta SL's FEI number?
- Antonio Garcia Inesta SL's FDA Establishment Identifier (FEI) is 3010145266.
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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.