Flavourtech (Offshore) S.A.L.
FDA import alert and refusal historyIzmir,Aegean, TurkeyFEI 2000018968
As of October 26, 2026, Flavourtech (Offshore) S.A.L. (Izmir,Aegean, Turkey) is on the red list of FDA Import Alert 45-02 (Foods with illegal or undeclared colors) for custard powder, published by FDA on January 20, 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 Flavourtech (Offshore) S.A.L.
2 records, newest first. Each line links to the FDA page it came from.
2016
- Import alert listingListed on Import Alert 45-02red listCustard PowderSource
2012
- InspectionInspection classified VAI (Voluntary Action Indicated)Foodborne Biological HazardsSource
Questions about Flavourtech (Offshore) S.A.L.
- Is Flavourtech (Offshore) S.A.L. on an FDA import alert?
- Yes. As of October 26, 2026, Flavourtech (Offshore) S.A.L. is on the red list of FDA Import Alert 45-02, “Foods with illegal or undeclared colors”, for custard powder; FDA published the listing on January 20, 2016.
- Has FDA refused shipments from Flavourtech (Offshore) S.A.L.?
- No FDA import refusals for Flavourtech (Offshore) S.A.L. appear in FDA's refusal data since October 2016, as of October 26, 2026.
- When was Flavourtech (Offshore) S.A.L. last inspected by FDA?
- FDA's most recent inspection of Flavourtech (Offshore) S.A.L. with a final classification is dated April 10, 2012 and was classified VAI (Voluntary Action Indicated).
- What is Flavourtech (Offshore) S.A.L.'s FEI number?
- Flavourtech (Offshore) S.A.L.'s FDA Establishment Identifier (FEI) is 2000018968.
- Can shipments from Flavourtech (Offshore) S.A.L. still enter the U.S.?
- Shipments of custard powder from Flavourtech (Offshore) S.A.L. 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.