Solea SRL
FDA import alert and refusal historySanta Maria La Carita, ItalyFEI 3007853329
As of October 25, 2026, Solea SRL is not on any FDA import alert in SupplierRadar's records; FDA refused 2 of its shipment lines on January 22, 2024, 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
- Tomatoes (fruit used as vegetable) · FILTHY
- Last warning letter
- None found
- Last inspection
- Classified VAI (Voluntary Action Indicated)
Every FDA record for Solea SRL
3 records, newest first. Each line links to the FDA page it came from.
2026
- InspectionInspection classified VAI (Voluntary Action Indicated)Food Composition, Standards, Labeling and Econ; Foodborne Biological HazardsSource
2024
Refusal charges, in plain English
- FILTHY2 refused lines
Filthy, putrid or decomposed substance
The product appeared to consist in whole or in part of a filthy, putrid, or decomposed substance, or to be otherwise unfit for food.
Questions about Solea SRL
- Is Solea SRL on an FDA import alert?
- No listing for Solea SRL appears in the FDA import alerts SupplierRadar checked on October 25, 2026. Country-wide alerts may still apply to its products; see the Italy page.
- Has FDA refused shipments from Solea SRL?
- Yes. FDA refused 2 shipment lines from Solea SRL on January 22, 2024. The most recent, on January 22, 2024, was tomatoes (fruit used as vegetable), charged as FILTHY (filthy, putrid or decomposed substance).
- Why did FDA refuse Solea SRL's shipments?
- The most frequent charge is FILTHY (filthy, putrid or decomposed substance, 2 lines).
- When was Solea SRL last inspected by FDA?
- FDA's most recent inspection of Solea SRL with a final classification is dated July 15, 2026 and was classified VAI (Voluntary Action Indicated).
- What is Solea SRL's FEI number?
- Solea SRL's FDA Establishment Identifier (FEI) is 3007853329.
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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.