Procesamiento Esp Exporter
FDA import alert and refusal historyCiudad De Mexico, MexicoFEI 3027374886
Recorded by FDA as PROCESAMIENTO ESP EXPORTER
As of October 25, 2026, Procesamiento Esp Exporter (Ciudad De Mexico, Mexico) is on the red list of FDA Import Alert 99-39 (Imported foods that appear to be misbranded) for duchess light tuna in water (canned), published by FDA on October 12, 2023, 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 99-39 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Procesamiento Esp Exporter
1 record, newest first. Each line links to the FDA page it came from.
2023
- Import alert listingListed on Import Alert 99-39red listDuchess Light Tuna in Water (Canned)Source
Questions about Procesamiento Esp Exporter
- Is Procesamiento Esp Exporter on an FDA import alert?
- Yes. As of October 25, 2026, Procesamiento Esp Exporter is on the red list of FDA Import Alert 99-39, “Imported foods that appear to be misbranded”, for duchess light tuna in water (canned); FDA published the listing on October 12, 2023.
- Has FDA refused shipments from Procesamiento Esp Exporter?
- No FDA import refusals for Procesamiento Esp Exporter appear in FDA's refusal data since October 2016, as of October 25, 2026.
- What is Procesamiento Esp Exporter's FEI number?
- Procesamiento Esp Exporter's FDA Establishment Identifier (FEI) is 3027374886.
- Can shipments from Procesamiento Esp Exporter still enter the U.S.?
- Shipments of duchess light tuna in water (canned) from Procesamiento Esp Exporter can be detained without physical examination under Import Alert 99-39; 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.