Productos Agricolas El Labrador
FDA import alert and refusal historyTepic, MexicoFEI 3004120561
As of October 26, 2026, Productos Agricolas El Labrador (Tepic, Mexico) is on the red list of FDA Import Alert 99-05 (Raw agricultural products: pesticides) for longbeans, raw, fresh, ambient; longbeans, raw, fresh, refrigerated; pepper, hot, n.e.c. (fruit used as vegetable), 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 Productos Agricolas El Labrador
1 record, newest first. Each line links to the FDA page it came from.
2009
- Import alert listingListed on Import Alert 99-05red listLongbeans, Raw, Fresh, Ambient; Longbeans, Raw, Fresh, Refrigerated; Pepper, Hot, N.E.C. (Fruit Used as Vegetable)Source
Questions about Productos Agricolas El Labrador
- Is Productos Agricolas El Labrador on an FDA import alert?
- Yes. As of October 26, 2026, Productos Agricolas El Labrador is on the red list of FDA Import Alert 99-05, “Raw agricultural products: pesticides”, for longbeans, raw, fresh, ambient; longbeans, raw, fresh, refrigerated; pepper, hot, n.e.c. (fruit used as vegetable); FDA published the listing on September 16, 2009.
- Has FDA refused shipments from Productos Agricolas El Labrador?
- No FDA import refusals for Productos Agricolas El Labrador appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Productos Agricolas El Labrador's FEI number?
- Productos Agricolas El Labrador's FDA Establishment Identifier (FEI) is 3004120561.
- Can shipments from Productos Agricolas El Labrador still enter the U.S.?
- Shipments of longbeans, raw, fresh, ambient; longbeans, raw, fresh, refrigerated; pepper, hot, n.e.c. (fruit used as vegetable) from Productos Agricolas El Labrador 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.