Miguel Gonzalez
FDA import alert and refusal historyGuadalajara, MexicoFEI 3006501175
As of October 25, 2026, Miguel Gonzalez (Guadalajara, Mexico) is on the red list of FDA Import Alert 45-02 (Foods with illegal or undeclared colors) for guava roll; guava, dried or paste; guava, jam, jelly, preserves, marmalade, butter or candied, 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 Miguel Gonzalez
1 record, newest first. Each line links to the FDA page it came from.
2009
- Import alert listingListed on Import Alert 45-02red listguava roll; Guava, Dried or Paste; Guava, Jam, Jelly, Preserves, Marmalade, Butter or CandiedSource
Questions about Miguel Gonzalez
- Is Miguel Gonzalez on an FDA import alert?
- Yes. As of October 25, 2026, Miguel Gonzalez is on the red list of FDA Import Alert 45-02, “Foods with illegal or undeclared colors”, for guava roll; guava, dried or paste; guava, jam, jelly, preserves, marmalade, butter or candied; FDA published the listing on September 18, 2009.
- Has FDA refused shipments from Miguel Gonzalez?
- No FDA import refusals for Miguel Gonzalez appear in FDA's refusal data since October 2016, as of October 25, 2026.
- What is Miguel Gonzalez's FEI number?
- Miguel Gonzalez's FDA Establishment Identifier (FEI) is 3006501175.
- Can shipments from Miguel Gonzalez still enter the U.S.?
- Shipments of guava roll; guava, dried or paste; guava, jam, jelly, preserves, marmalade, butter or candied from Miguel Gonzalez 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.