Lindt & Sprungli SpA
FDA import alert and refusal historyLuserna San Giovanni, ItalyFEI 1000289784
As of October 26, 2026, Lindt & Sprungli SpA (Luserna San Giovanni, Italy) is on the red list of FDA Import Alert 45-02 (Foods with illegal or undeclared colors) for loose jelly candies, published by FDA on December 13, 2016, and has no FDA import refusals recorded since October 2016.
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- IA 45-02 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- Classified VAI (Voluntary Action Indicated)
Every FDA record for Lindt & Sprungli SpA
3 records, newest first. Each line links to the FDA page it came from.
2019
- InspectionInspection classified VAI (Voluntary Action Indicated)Food Composition, Standards, Labeling and Econ; Foodborne Biological HazardsSource
2016
- Import alert listingListed on Import Alert 45-02red listLoose Jelly CandiesSource
2014
- InspectionInspection classified VAI (Voluntary Action Indicated)Foodborne Biological HazardsSource
Questions about Lindt & Sprungli SpA
- Is Lindt & Sprungli SpA on an FDA import alert?
- Yes. As of October 26, 2026, Lindt & Sprungli SpA is on the red list of FDA Import Alert 45-02, “Foods with illegal or undeclared colors”, for loose jelly candies; FDA published the listing on December 13, 2016.
- Has FDA refused shipments from Lindt & Sprungli SpA?
- No FDA import refusals for Lindt & Sprungli SpA appear in FDA's refusal data since October 2016, as of October 26, 2026.
- When was Lindt & Sprungli SpA last inspected by FDA?
- FDA's most recent inspection of Lindt & Sprungli SpA with a final classification is dated June 6, 2019 and was classified VAI (Voluntary Action Indicated).
- What is Lindt & Sprungli SpA's FEI number?
- Lindt & Sprungli SpA's FDA Establishment Identifier (FEI) is 1000289784.
- Can shipments from Lindt & Sprungli SpA still enter the U.S.?
- Shipments of loose jelly candies from Lindt & Sprungli SpA can be detained without physical examination under Import Alert 45-02; FDA releases them only if evidence shows they do not have the listed violation. Importers must consider this listing in their FSVP evaluation (21 CFR 1.505).
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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.