Comercializadora de Productos de Importacion y Exportacion
FDA import alert and refusal historyTijuana, MexicoFEI 2000043299
As of October 26, 2026, Comercializadora de Productos de Importacion y Exportacion (Tijuana, Mexico) is on the red list of FDA Import Alert 99-23 (Produce: contamination with human pathogens) for serrano peppers, published by FDA on January 18, 2011, 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 99-23 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Comercializadora de Productos de Importacion y Exportacion
1 record, newest first. Each line links to the FDA page it came from.
2011
- Import alert listingListed on Import Alert 99-23red listSerrano PeppersSource
Questions about Comercializadora de Productos de Importacion y Exportacion
- Is Comercializadora de Productos de Importacion y Exportacion on an FDA import alert?
- Yes. As of October 26, 2026, Comercializadora de Productos de Importacion y Exportacion is on the red list of FDA Import Alert 99-23, “Produce: contamination with human pathogens”, for serrano peppers; FDA published the listing on January 18, 2011.
- Has FDA refused shipments from Comercializadora de Productos de Importacion y Exportacion?
- No FDA import refusals for Comercializadora de Productos de Importacion y Exportacion appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Comercializadora de Productos de Importacion y Exportacion's FEI number?
- Comercializadora de Productos de Importacion y Exportacion's FDA Establishment Identifier (FEI) is 2000043299.
- Can shipments from Comercializadora de Productos de Importacion y Exportacion still enter the U.S.?
- Shipments of serrano peppers from Comercializadora de Productos de Importacion y Exportacion can be detained without physical examination under Import Alert 99-23; 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.