Efren Diaz Pelayo
FDA import alert and refusal historyBaja California, MexicoFEI 3007029593
As of October 26, 2026, Efren Diaz Pelayo (Baja California, Mexico) is on the red list of FDA Import Alert 99-05 (Raw agricultural products: pesticides) for serrano pepper, hot (fruit used as vegetable), raw, fresh, ambient; serrano pepper, hot (fruit used as vegetable), raw, fresh, refrigerated, published by FDA on September 30, 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 Efren Diaz Pelayo
1 record, newest first. Each line links to the FDA page it came from.
2009
- Import alert listingListed on Import Alert 99-05red listSerrano Pepper, Hot (Fruit Used as Vegetable), Raw, Fresh, Ambient; Serrano Pepper, Hot (Fruit Used as Vegetable), Raw, Fresh, RefrigeratedSource
Questions about Efren Diaz Pelayo
- Is Efren Diaz Pelayo on an FDA import alert?
- Yes. As of October 26, 2026, Efren Diaz Pelayo is on the red list of FDA Import Alert 99-05, “Raw agricultural products: pesticides”, for serrano pepper, hot (fruit used as vegetable), raw, fresh, ambient; serrano pepper, hot (fruit used as vegetable), raw, fresh, refrigerated; FDA published the listing on September 30, 2009.
- Has FDA refused shipments from Efren Diaz Pelayo?
- No FDA import refusals for Efren Diaz Pelayo appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Efren Diaz Pelayo's FEI number?
- Efren Diaz Pelayo's FDA Establishment Identifier (FEI) is 3007029593.
- Can shipments from Efren Diaz Pelayo still enter the U.S.?
- Shipments of serrano pepper, hot (fruit used as vegetable), raw, fresh, ambient; serrano pepper, hot (fruit used as vegetable), raw, fresh, refrigerated from Efren Diaz Pelayo 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.