Productor Y Distribuidores De Guazontles, Cebolla Cambray, P
FDA import alert and refusal historyLos Reyes De Jurez, MexicoFEI 3010690691
As of October 27, 2026, Productor Y Distribuidores De Guazontles, Cebolla Cambray, P (Los Reyes De Jurez, Mexico) is on the red list of FDA Import Alert 99-05 (Raw agricultural products: pesticides) for green onions, published by FDA on April 28, 2015, 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 99-05 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Productor Y Distribuidores De Guazontles, Cebolla Cambray, P
1 record, newest first. Each line links to the FDA page it came from.
2015
- Import alert listingListed on Import Alert 99-05red listGreen OnionsSource
Questions about Productor Y Distribuidores De Guazontles, Cebolla Cambray, P
- Is Productor Y Distribuidores De Guazontles, Cebolla Cambray, P on an FDA import alert?
- Yes. As of October 27, 2026, Productor Y Distribuidores De Guazontles, Cebolla Cambray, P is on the red list of FDA Import Alert 99-05, “Raw agricultural products: pesticides”, for green onions; FDA published the listing on April 28, 2015.
- Has FDA refused shipments from Productor Y Distribuidores De Guazontles, Cebolla Cambray, P?
- No FDA import refusals for Productor Y Distribuidores De Guazontles, Cebolla Cambray, P appear in FDA's refusal data since October 2016, as of October 27, 2026.
- What is Productor Y Distribuidores De Guazontles, Cebolla Cambray, P's FEI number?
- Productor Y Distribuidores De Guazontles, Cebolla Cambray, P's FDA Establishment Identifier (FEI) is 3010690691.
- Can shipments from Productor Y Distribuidores De Guazontles, Cebolla Cambray, P still enter the U.S.?
- Shipments of green onions from Productor Y Distribuidores De Guazontles, Cebolla Cambray, P 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.