Frutas y Hortalizas Naces SA
FDA import alert and refusal historyRoquetas De Mar, SpainFEI 3004397085
As of October 26, 2026, Frutas y Hortalizas Naces SA (Roquetas De Mar, Spain) is on the red list of FDA Import Alert 99-05 (Raw agricultural products: pesticides) for cucumbers (fruit used as vegetable), raw, fresh, ambient; cucumbers (fruit used as vegetable), 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 Frutas y Hortalizas Naces SA
1 record, newest first. Each line links to the FDA page it came from.
2009
- Import alert listingListed on Import Alert 99-05red listCucumbers (Fruit Used as Vegetable), Raw, Fresh, Ambient; Cucumbers (Fruit Used as Vegetable), Raw, Fresh, RefrigeratedSource
Questions about Frutas y Hortalizas Naces SA
- Is Frutas y Hortalizas Naces SA on an FDA import alert?
- Yes. As of October 26, 2026, Frutas y Hortalizas Naces SA is on the red list of FDA Import Alert 99-05, “Raw agricultural products: pesticides”, for cucumbers (fruit used as vegetable), raw, fresh, ambient; cucumbers (fruit used as vegetable), raw, fresh, refrigerated; FDA published the listing on September 16, 2009.
- Has FDA refused shipments from Frutas y Hortalizas Naces SA?
- No FDA import refusals for Frutas y Hortalizas Naces SA appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Frutas y Hortalizas Naces SA's FEI number?
- Frutas y Hortalizas Naces SA's FDA Establishment Identifier (FEI) is 3004397085.
- Can shipments from Frutas y Hortalizas Naces SA still enter the U.S.?
- Shipments of cucumbers (fruit used as vegetable), raw, fresh, ambient; cucumbers (fruit used as vegetable), raw, fresh, refrigerated from Frutas y Hortalizas Naces SA 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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