Rancho Santiago de Acozac SA de CV
FDA import alert and refusal historyAcozac Pue, MexicoFEI 3008438105
Recorded by FDA as RANCHO SANTIAGO DE ACOZAC SA DE CV
As of October 26, 2026, Rancho Santiago de Acozac SA de CV (Acozac Pue, Mexico) is on the red list of FDA Import Alert 99-21 (Foods with undeclared added sulfiting agents) for fruit and vegetable mix, published by FDA on March 18, 2010, is also listed on Import Alert 99-05 (red list), 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 99-21 · red listIA 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 Rancho Santiago de Acozac SA de CV
2 records, newest first. Each line links to the FDA page it came from.
2010
- Import alert listingListed on Import Alert 99-21red listFruit and Vegetable MixSource
2009
- Import alert listingListed on Import Alert 99-05red listFresh Green Onions; Aztech Spinach (Guazontle)Source
Questions about Rancho Santiago de Acozac SA de CV
- Is Rancho Santiago de Acozac SA de CV on an FDA import alert?
- Yes. As of October 26, 2026, Rancho Santiago de Acozac SA de CV is on the red list of FDA Import Alert 99-21, “Foods with undeclared added sulfiting agents”, for fruit and vegetable mix; FDA published the listing on March 18, 2010.
- Has FDA refused shipments from Rancho Santiago de Acozac SA de CV?
- No FDA import refusals for Rancho Santiago de Acozac SA de CV appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Rancho Santiago de Acozac SA de CV's FEI number?
- Rancho Santiago de Acozac SA de CV's FDA Establishment Identifier (FEI) is 3008438105.
- Can shipments from Rancho Santiago de Acozac SA de CV still enter the U.S.?
- Shipments of fruit and vegetable mix from Rancho Santiago de Acozac SA de CV can be detained without physical examination under Import Alert 99-21; 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.