Exportadora Melgon
FDA import alert and refusal historyVilla Nueva, GuatemalaFEI 3005065244
As of October 26, 2026, Exportadora Melgon (Villa Nueva, Guatemala) is on the red list of FDA Import Alert 99-05 (Raw agricultural products: pesticides) for pineapple (subtropical and tropical fruit), raw, fresh, ambient; pineapple (subtropical and tropical fruit), raw, fresh, refrigerated, 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 Exportadora Melgon
1 record, newest first. Each line links to the FDA page it came from.
2009
- Import alert listingListed on Import Alert 99-05red listPineapple (Subtropical and Tropical Fruit), Raw, Fresh, Ambient; Pineapple (Subtropical and Tropical Fruit), Raw, Fresh, RefrigeratedSource
Questions about Exportadora Melgon
- Is Exportadora Melgon on an FDA import alert?
- Yes. As of October 26, 2026, Exportadora Melgon is on the red list of FDA Import Alert 99-05, “Raw agricultural products: pesticides”, for pineapple (subtropical and tropical fruit), raw, fresh, ambient; pineapple (subtropical and tropical fruit), raw, fresh, refrigerated; FDA published the listing on September 16, 2009.
- Has FDA refused shipments from Exportadora Melgon?
- No FDA import refusals for Exportadora Melgon appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Exportadora Melgon's FEI number?
- Exportadora Melgon's FDA Establishment Identifier (FEI) is 3005065244.
- Can shipments from Exportadora Melgon still enter the U.S.?
- Shipments of pineapple (subtropical and tropical fruit), raw, fresh, ambient; pineapple (subtropical and tropical fruit), raw, fresh, refrigerated from Exportadora Melgon 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.