Oscar Atempan Galindo
FDA import alert and refusal historyLos Reyes de Juarez, MexicoFEI 3013569630
Recorded by FDA as OSCAR ATEMPAN GALINDO
As of October 26, 2026, Oscar Atempan Galindo (Los Reyes de Juarez, Mexico) is on the red list of FDA Import Alert 99-05 (Raw agricultural products: pesticides) for radish, published by FDA on December 1, 2023, 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
- Radish (root & tuber vegetable) · PESTICIDE
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Oscar Atempan Galindo
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 Oscar Atempan Galindo
- Is Oscar Atempan Galindo on an FDA import alert?
- Yes. As of October 26, 2026, Oscar Atempan Galindo is on the red list of FDA Import Alert 99-05, “Raw agricultural products: pesticides”, for radish; FDA published the listing on December 1, 2023.
- Has FDA refused shipments from Oscar Atempan Galindo?
- Yes. FDA refused 2 shipment lines from Oscar Atempan Galindo between July 24, 2017 and November 25, 2023. The most recent, on November 25, 2023, was radish (root & tuber vegetable), charged as PESTICIDE (pesticide chemical residue).
- Why did FDA refuse Oscar Atempan Galindo's shipments?
- The most frequent charge is PESTICIDE (pesticide chemical residue, 2 lines).
- What is Oscar Atempan Galindo's FEI number?
- Oscar Atempan Galindo's FDA Establishment Identifier (FEI) is 3013569630.
- Can shipments from Oscar Atempan Galindo still enter the U.S.?
- Shipments of radish from Oscar Atempan Galindo 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.