Empaque de Frutas Chulavista S.A. de C.V.
FDA import alert and refusal historyTecoman, MexicoFEI 3007559617
As of October 27, 2026, Empaque de Frutas Chulavista S.A. de C.V. (Tecoman, Mexico) is on the red list of FDA Import Alert 99-23 (Produce: contamination with human pathogens) for papaya, published by FDA on August 10, 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 Empaque de Frutas Chulavista S.A. de C.V.
1 record, newest first. Each line links to the FDA page it came from.
2011
- Import alert listingListed on Import Alert 99-23red listPapayaSource
Questions about Empaque de Frutas Chulavista S.A. de C.V.
- Is Empaque de Frutas Chulavista S.A. de C.V. on an FDA import alert?
- Yes. As of October 27, 2026, Empaque de Frutas Chulavista S.A. de C.V. is on the red list of FDA Import Alert 99-23, “Produce: contamination with human pathogens”, for papaya; FDA published the listing on August 10, 2011.
- Has FDA refused shipments from Empaque de Frutas Chulavista S.A. de C.V.?
- No FDA import refusals for Empaque de Frutas Chulavista S.A. de C.V. appear in FDA's refusal data since October 2016, as of October 27, 2026.
- What is Empaque de Frutas Chulavista S.A. de C.V.'s FEI number?
- Empaque de Frutas Chulavista S.A. de C.V.'s FDA Establishment Identifier (FEI) is 3007559617.
- Can shipments from Empaque de Frutas Chulavista S.A. de C.V. still enter the U.S.?
- Shipments of papaya from Empaque de Frutas Chulavista S.A. de C.V. 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.