Grupo Villalori SA de CV
FDA import alert and refusal historySantiago De Queretaro, MexicoFEI 3011314407
Recorded by FDA as GRUPO VILLALORI SA DE CV
As of October 26, 2026, Grupo Villalori SA de CV (Santiago De Queretaro, Mexico) is on the red list of FDA Import Alert 99-05 (Raw agricultural products: pesticides) for fresh greenhouse super sweet mini peppers, published by FDA on August 17, 2016, 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 Grupo Villalori SA de CV
1 record, newest first. Each line links to the FDA page it came from.
2016
- Import alert listingListed on Import Alert 99-05red listFresh greenhouse super sweet mini peppersSource
Questions about Grupo Villalori SA de CV
- Is Grupo Villalori SA de CV on an FDA import alert?
- Yes. As of October 26, 2026, Grupo Villalori SA de CV is on the red list of FDA Import Alert 99-05, “Raw agricultural products: pesticides”, for fresh greenhouse super sweet mini peppers; FDA published the listing on August 17, 2016.
- Has FDA refused shipments from Grupo Villalori SA de CV?
- No FDA import refusals for Grupo Villalori SA de CV appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Grupo Villalori SA de CV's FEI number?
- Grupo Villalori SA de CV's FDA Establishment Identifier (FEI) is 3011314407.
- Can shipments from Grupo Villalori SA de CV still enter the U.S.?
- Shipments of fresh greenhouse super sweet mini peppers from Grupo Villalori SA de CV 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.