Ravico SA
FDA import alert and refusal historyLonderzeel, BelgiumFEI 3002815247
As of October 25, 2026, Ravico SA (Londerzeel, Belgium) is on the red list of FDA Import Alert 45-02 (Foods with illegal or undeclared colors) for candy satellite wafer, published by FDA on September 18, 2009, 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 Ravico SA
2 records, newest first. Each line links to the FDA page it came from.
2016
- InspectionInspection classified VAI (Voluntary Action Indicated)Foodborne Biological HazardsSource
2009
- Import alert listingListed on Import Alert 45-02red listcandy satellite waferSource
Questions about Ravico SA
- Is Ravico SA on an FDA import alert?
- Yes. As of October 25, 2026, Ravico SA is on the red list of FDA Import Alert 45-02, “Foods with illegal or undeclared colors”, for candy satellite wafer; FDA published the listing on September 18, 2009.
- Has FDA refused shipments from Ravico SA?
- No FDA import refusals for Ravico SA appear in FDA's refusal data since October 2016, as of October 25, 2026.
- When was Ravico SA last inspected by FDA?
- FDA's most recent inspection of Ravico SA with a final classification is dated November 30, 2016 and was classified VAI (Voluntary Action Indicated).
- What is Ravico SA's FEI number?
- Ravico SA's FDA Establishment Identifier (FEI) is 3002815247.
- Can shipments from Ravico SA still enter the U.S.?
- Shipments of candy satellite wafer from Ravico SA 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.