Sunnyland
FDA import alert and refusal historyTurnhout, BelgiumFEI 3011281386
As of October 26, 2026, Sunnyland (Turnhout, Belgium) is on the red list of FDA Import Alert 99-39 (Imported foods that appear to be misbranded) for guava juice drink; mango juice drink; lychee juice drink, published by FDA on August 5, 2015, 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 99-39 · 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 Sunnyland
2 records, newest first. Each line links to the FDA page it came from.
2015
- Import alert listingListed on Import Alert 99-39red listGuava Juice Drink; Mango Juice Drink; Lychee Juice DrinkSource
2013
- InspectionInspection classified VAI (Voluntary Action Indicated)Foodborne Biological HazardsSource
Questions about Sunnyland
- Is Sunnyland on an FDA import alert?
- Yes. As of October 26, 2026, Sunnyland is on the red list of FDA Import Alert 99-39, “Imported foods that appear to be misbranded”, for guava juice drink; mango juice drink; lychee juice drink; FDA published the listing on August 5, 2015.
- Has FDA refused shipments from Sunnyland?
- No FDA import refusals for Sunnyland appear in FDA's refusal data since October 2016, as of October 26, 2026.
- When was Sunnyland last inspected by FDA?
- FDA's most recent inspection of Sunnyland with a final classification is dated March 5, 2013 and was classified VAI (Voluntary Action Indicated).
- What is Sunnyland's FEI number?
- Sunnyland's FDA Establishment Identifier (FEI) is 3011281386.
- Can shipments from Sunnyland still enter the U.S.?
- Shipments of guava juice drink; mango juice drink; lychee juice drink from Sunnyland can be detained without physical examination under Import Alert 99-39; 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.