Productos la mestizota s de rl de cv
FDA import alert and refusal historyCuliacan, MexicoFEI 3010098089
As of October 26, 2026, Productos la mestizota s de rl de cv (Culiacan, Mexico) is on the red list of FDA Import Alert 45-02 (Foods with illegal or undeclared colors) for guava pie (turnover with guava), published by FDA on September 4, 2013, 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 Productos la mestizota s de rl de cv
1 record, newest first. Each line links to the FDA page it came from.
2013
- Import alert listingListed on Import Alert 45-02red listGuava Pie (Turnover with Guava)Source
Questions about Productos la mestizota s de rl de cv
- Is Productos la mestizota s de rl de cv on an FDA import alert?
- Yes. As of October 26, 2026, Productos la mestizota s de rl de cv is on the red list of FDA Import Alert 45-02, “Foods with illegal or undeclared colors”, for guava pie (turnover with guava); FDA published the listing on September 4, 2013.
- Has FDA refused shipments from Productos la mestizota s de rl de cv?
- No FDA import refusals for Productos la mestizota s de rl de cv appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Productos la mestizota s de rl de cv's FEI number?
- Productos la mestizota s de rl de cv's FDA Establishment Identifier (FEI) is 3010098089.
- Can shipments from Productos la mestizota s de rl de cv still enter the U.S.?
- Shipments of guava pie (turnover with guava) from Productos la mestizota s de rl de cv 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.