Grace Kennedy Export Trading Ltd
FDA import alert and refusal historyKingston, JamaicaFEI 1000207159
As of October 26, 2026, Grace Kennedy Export Trading Ltd (Kingston, Jamaica) is on the red list of FDA Import Alert 45-02 (Foods with illegal or undeclared colors) for soft drink, citrus fruit flavored, carbonated, published by FDA on September 18, 2009, is also listed on Import Alert 99-19 (red list), 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 listIA 99-19 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Grace Kennedy Export Trading Ltd
2 records, newest first. Each line links to the FDA page it came from.
2009
- Import alert listingListed on Import Alert 45-02red listSoft Drink, Citrus Fruit Flavored, CarbonatedSource
- Import alert listingListed on Import Alert 99-19red listcerasee teaSource
Questions about Grace Kennedy Export Trading Ltd
- Is Grace Kennedy Export Trading Ltd on an FDA import alert?
- Yes. As of October 26, 2026, Grace Kennedy Export Trading Ltd is on the red list of FDA Import Alert 45-02, “Foods with illegal or undeclared colors”, for soft drink, citrus fruit flavored, carbonated; FDA published the listing on September 18, 2009.
- Has FDA refused shipments from Grace Kennedy Export Trading Ltd?
- No FDA import refusals for Grace Kennedy Export Trading Ltd appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Grace Kennedy Export Trading Ltd's FEI number?
- Grace Kennedy Export Trading Ltd's FDA Establishment Identifier (FEI) is 1000207159.
- Can shipments from Grace Kennedy Export Trading Ltd still enter the U.S.?
- Shipments of soft drink, citrus fruit flavored, carbonated from Grace Kennedy Export Trading Ltd 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.