Amanda Iturbide Conde
FDA import alert and refusal historyAtoyatempam, MexicoFEI 3037649658
Recorded by FDA as AMANDA ITURBIDE CONDE
As of October 26, 2026, Amanda Iturbide Conde (Atoyatempam, Mexico) is on the red list of FDA Import Alert 99-05 (Raw agricultural products: pesticides) for green beans, published by FDA on September 9, 2026, and has 2 FDA import refusals recorded since October 2016.
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- IA 99-05 · red list
- Last import refusal
- Stringbeans · PESTICIDE
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Amanda Iturbide Conde
3 records, newest first. Each line links to the FDA page it came from.
Refusal charges, in plain English
- PESTICIDE2 refused lines
Pesticide chemical residue
The product appeared to contain a pesticide chemical residue that makes it adulterated under section 402(a)(2)(B) of the FD&C Act, for example a residue above the U.S. tolerance or one with no U.S. tolerance for that food.
Questions about Amanda Iturbide Conde
- Is Amanda Iturbide Conde on an FDA import alert?
- Yes. As of October 26, 2026, Amanda Iturbide Conde is on the red list of FDA Import Alert 99-05, “Raw agricultural products: pesticides”, for green beans; FDA published the listing on September 9, 2026.
- Has FDA refused shipments from Amanda Iturbide Conde?
- Yes. FDA refused 2 shipment lines from Amanda Iturbide Conde between May 11, 2026 and June 4, 2026. The most recent, on June 4, 2026, was stringbeans, charged as PESTICIDE (pesticide chemical residue).
- Why did FDA refuse Amanda Iturbide Conde's shipments?
- The most frequent charge is PESTICIDE (pesticide chemical residue, 2 lines).
- What is Amanda Iturbide Conde's FEI number?
- Amanda Iturbide Conde's FDA Establishment Identifier (FEI) is 3037649658.
- Can shipments from Amanda Iturbide Conde still enter the U.S.?
- Shipments of green beans from Amanda Iturbide Conde can be detained without physical examination under Import Alert 99-05; 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.