Intermediadora de Frutas, S. A. de C.V.
FDA import alert and refusal historyMerida, MexicoFEI 3004265399
As of October 26, 2026, Intermediadora de Frutas, S. A. de C.V. (Merida, Mexico) is on the red list of FDA Import Alert 99-05 (Raw agricultural products: pesticides) for papaya (papaw) (subtropical and tropical fruit), published by FDA on September 16, 2009, 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 Intermediadora de Frutas, S. A. de C.V.
1 record, newest first. Each line links to the FDA page it came from.
2009
- Import alert listingListed on Import Alert 99-05red listPapaya (Papaw) (Subtropical and Tropical Fruit)Source
Questions about Intermediadora de Frutas, S. A. de C.V.
- Is Intermediadora de Frutas, S. A. de C.V. on an FDA import alert?
- Yes. As of October 26, 2026, Intermediadora de Frutas, S. A. de C.V. is on the red list of FDA Import Alert 99-05, “Raw agricultural products: pesticides”, for papaya (papaw) (subtropical and tropical fruit); FDA published the listing on September 16, 2009.
- Has FDA refused shipments from Intermediadora de Frutas, S. A. de C.V.?
- No FDA import refusals for Intermediadora de Frutas, S. A. de C.V. appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Intermediadora de Frutas, S. A. de C.V.'s FEI number?
- Intermediadora de Frutas, S. A. de C.V.'s FDA Establishment Identifier (FEI) is 3004265399.
- Can shipments from Intermediadora de Frutas, S. A. de C.V. still enter the U.S.?
- Shipments of papaya (papaw) (subtropical and tropical fruit) from Intermediadora de Frutas, S. A. de C.V. 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.