Nat's Veggies Produce SPR DE RL DE CV/ Gena Produce SA DE CV
FDA import alert and refusal historyEnsenada, MexicoFEI 3009875771
As of October 26, 2026, Nat's Veggies Produce SPR DE RL DE CV/ Gena Produce SA DE CV (Ensenada, Mexico) is on the red list of FDA Import Alert 99-05 (Raw agricultural products: pesticides) for green beans; red beets, published by FDA on August 20, 2013, 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 Nat's Veggies Produce SPR DE RL DE CV/ Gena Produce SA DE CV
1 record, newest first. Each line links to the FDA page it came from.
2013
- Import alert listingListed on Import Alert 99-05red listGreen Beans; Red BeetsSource
Questions about Nat's Veggies Produce SPR DE RL DE CV/ Gena Produce SA DE CV
- Is Nat's Veggies Produce SPR DE RL DE CV/ Gena Produce SA DE CV on an FDA import alert?
- Yes. As of October 26, 2026, Nat's Veggies Produce SPR DE RL DE CV/ Gena Produce SA DE CV is on the red list of FDA Import Alert 99-05, “Raw agricultural products: pesticides”, for green beans; red beets; FDA published the listing on August 20, 2013.
- Has FDA refused shipments from Nat's Veggies Produce SPR DE RL DE CV/ Gena Produce SA DE CV?
- No FDA import refusals for Nat's Veggies Produce SPR DE RL DE CV/ Gena Produce SA DE CV appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Nat's Veggies Produce SPR DE RL DE CV/ Gena Produce SA DE CV's FEI number?
- Nat's Veggies Produce SPR DE RL DE CV/ Gena Produce SA DE CV's FDA Establishment Identifier (FEI) is 3009875771.
- Can shipments from Nat's Veggies Produce SPR DE RL DE CV/ Gena Produce SA DE CV still enter the U.S.?
- Shipments of green beans; red beets from Nat's Veggies Produce SPR DE RL DE CV/ Gena Produce SA DE CV 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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