Catalina Diaz Beltran
FDA import alert and refusal historyEnsenada, MexicoFEI 3004315839
Recorded by FDA as CATALINA DIAZ BELTRAN
As of October 26, 2026, Catalina Diaz Beltran (Ensenada, Mexico) is on the red list of FDA Import Alert 99-05 (Raw agricultural products: pesticides) for beets; golden; root & tuber vegetable, n.e.c., raw, fresh, ambient; root & tuber vegetable, n.e.c., 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 Catalina Diaz Beltran
1 record, newest first. Each line links to the FDA page it came from.
2009
- Import alert listingListed on Import Alert 99-05red listBeets; golden; Root & Tuber Vegetable, N.E.C., Raw, Fresh, Ambient; Root & Tuber Vegetable, N.E.C., Raw, Fresh, RefrigeratedSource
Questions about Catalina Diaz Beltran
- Is Catalina Diaz Beltran on an FDA import alert?
- Yes. As of October 26, 2026, Catalina Diaz Beltran is on the red list of FDA Import Alert 99-05, “Raw agricultural products: pesticides”, for beets; golden; root & tuber vegetable, n.e.c., raw, fresh, ambient; root & tuber vegetable, n.e.c., raw, fresh, refrigerated; FDA published the listing on September 16, 2009.
- Has FDA refused shipments from Catalina Diaz Beltran?
- No FDA import refusals for Catalina Diaz Beltran appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Catalina Diaz Beltran's FEI number?
- Catalina Diaz Beltran's FDA Establishment Identifier (FEI) is 3004315839.
- Can shipments from Catalina Diaz Beltran still enter the U.S.?
- Shipments of beets; golden; root & tuber vegetable, n.e.c., raw, fresh, ambient; root & tuber vegetable, n.e.c., raw, fresh, refrigerated from Catalina Diaz Beltran 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.