comercializadora interveggie s.a. de c.v.
FDA import alert and refusal historyCuliacan, MexicoFEI 3006347818
As of October 26, 2026, comercializadora interveggie s.a. de c.v. (Culiacan, Mexico) is on the red list of FDA Import Alert 99-05 (Raw agricultural products: pesticides) for stringbeans, raw, fresh, ambient; stringbeans, 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 comercializadora interveggie s.a. de c.v.
1 record, newest first. Each line links to the FDA page it came from.
2009
- Import alert listingListed on Import Alert 99-05red listStringbeans, Raw, Fresh, Ambient; Stringbeans, Raw, Fresh, RefrigeratedSource
Questions about comercializadora interveggie s.a. de c.v.
- Is comercializadora interveggie s.a. de c.v. on an FDA import alert?
- Yes. As of October 26, 2026, comercializadora interveggie s.a. de c.v. is on the red list of FDA Import Alert 99-05, “Raw agricultural products: pesticides”, for stringbeans, raw, fresh, ambient; stringbeans, raw, fresh, refrigerated; FDA published the listing on September 16, 2009.
- Has FDA refused shipments from comercializadora interveggie s.a. de c.v.?
- No FDA import refusals for comercializadora interveggie s.a. de c.v. appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is comercializadora interveggie s.a. de c.v.'s FEI number?
- comercializadora interveggie s.a. de c.v.'s FDA Establishment Identifier (FEI) is 3006347818.
- Can shipments from comercializadora interveggie s.a. de c.v. still enter the U.S.?
- Shipments of stringbeans, raw, fresh, ambient; stringbeans, raw, fresh, refrigerated from comercializadora interveggie s.a. de c.v. 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.