Industrias Hermanos Juan Lopez
FDA import alert and refusal historyMontijo, SpainFEI 3014836921
Recorded by FDA as INDUSTRIAS HERMANOS JUAN LOPEZ
As of October 26, 2026, Industrias Hermanos Juan Lopez (Montijo, Spain) is on the red list of FDA Import Alert 45-02 (Foods with illegal or undeclared colors) for lollipop (without chocolate); candy specialties, n.e.c. (without chocolate), 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 Industrias Hermanos Juan Lopez
1 record, newest first. Each line links to the FDA page it came from.
2009
- Import alert listingListed on Import Alert 45-02red listLollipop (without Chocolate); Candy Specialties, N.E.C. (without Chocolate)Source
Questions about Industrias Hermanos Juan Lopez
- Is Industrias Hermanos Juan Lopez on an FDA import alert?
- Yes. As of October 26, 2026, Industrias Hermanos Juan Lopez is on the red list of FDA Import Alert 45-02, “Foods with illegal or undeclared colors”, for lollipop (without chocolate); candy specialties, n.e.c. (without chocolate); FDA published the listing on September 18, 2009.
- Has FDA refused shipments from Industrias Hermanos Juan Lopez?
- No FDA import refusals for Industrias Hermanos Juan Lopez appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Industrias Hermanos Juan Lopez's FEI number?
- Industrias Hermanos Juan Lopez's FDA Establishment Identifier (FEI) is 3014836921.
- Can shipments from Industrias Hermanos Juan Lopez still enter the U.S.?
- Shipments of lollipop (without chocolate); candy specialties, n.e.c. (without chocolate) from Industrias Hermanos Juan Lopez 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.