Suthera Enterprise Co,.Ltd
FDA import alert and refusal historyKanchanaburi, ThailandFEI 3007996820
As of October 25, 2026, Suthera Enterprise Co,.Ltd (Kanchanaburi, Thailand) is on the red list of FDA Import Alert 45-02 (Foods with illegal or undeclared colors) for coconut roll pandanus flavor, published by FDA on November 6, 2012, 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 Suthera Enterprise Co,.Ltd
2 records, newest first. Each line links to the FDA page it came from.
2012
- Import alert listingListed on Import Alert 45-02red listCoconut Roll Pandanus FlavorSource
2011
- InspectionInspection classified VAI (Voluntary Action Indicated)Foodborne Biological HazardsSource
Questions about Suthera Enterprise Co,.Ltd
- Is Suthera Enterprise Co,.Ltd on an FDA import alert?
- Yes. As of October 25, 2026, Suthera Enterprise Co,.Ltd is on the red list of FDA Import Alert 45-02, “Foods with illegal or undeclared colors”, for coconut roll pandanus flavor; FDA published the listing on November 6, 2012.
- Has FDA refused shipments from Suthera Enterprise Co,.Ltd?
- No FDA import refusals for Suthera Enterprise Co,.Ltd appear in FDA's refusal data since October 2016, as of October 25, 2026.
- When was Suthera Enterprise Co,.Ltd last inspected by FDA?
- FDA's most recent inspection of Suthera Enterprise Co,.Ltd with a final classification is dated June 8, 2011 and was classified VAI (Voluntary Action Indicated).
- What is Suthera Enterprise Co,.Ltd's FEI number?
- Suthera Enterprise Co,.Ltd's FDA Establishment Identifier (FEI) is 3007996820.
- Can shipments from Suthera Enterprise Co,.Ltd still enter the U.S.?
- Shipments of coconut roll pandanus flavor from Suthera Enterprise Co,.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.