Biscuitere Eugene Blond
FDA import alert and refusal historyLambersart, FranceFEI 3003487496
As of October 26, 2026, Biscuitere Eugene Blond (Lambersart, France) is on the red list of FDA Import Alert 45-02 (Foods with illegal or undeclared colors) for vanilla filled/iced cookies,biscuits and wafers; creme filled/iced cookie,biscuit,wafer; filled/iced cookies,biscuits and wafers, n.e.c., 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
- None on record
Every FDA record for Biscuitere Eugene Blond
1 record, newest first. Each line links to the FDA page it came from.
2009
- Import alert listingListed on Import Alert 45-02red listVanilla Filled/Iced Cookies,Biscuits and Wafers; Creme Filled/Iced Cookie,Biscuit,Wafer; Filled/Iced Cookies,Biscuits and Wafers, N.E.C.Source
Questions about Biscuitere Eugene Blond
- Is Biscuitere Eugene Blond on an FDA import alert?
- Yes. As of October 26, 2026, Biscuitere Eugene Blond is on the red list of FDA Import Alert 45-02, “Foods with illegal or undeclared colors”, for vanilla filled/iced cookies,biscuits and wafers; creme filled/iced cookie,biscuit,wafer; filled/iced cookies,biscuits and wafers, n.e.c.; FDA published the listing on September 18, 2009.
- Has FDA refused shipments from Biscuitere Eugene Blond?
- No FDA import refusals for Biscuitere Eugene Blond appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Biscuitere Eugene Blond's FEI number?
- Biscuitere Eugene Blond's FDA Establishment Identifier (FEI) is 3003487496.
- Can shipments from Biscuitere Eugene Blond still enter the U.S.?
- Shipments of vanilla filled/iced cookies,biscuits and wafers; creme filled/iced cookie,biscuit,wafer; filled/iced cookies,biscuits and wafers, n.e.c. from Biscuitere Eugene Blond 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.