Fruvemex Mexicali, S.A. de C.V.
FDA import alert and refusal historyPlayas De Rosarito, MexicoFEI 3013125433
As of October 27, 2026, Fruvemex Mexicali, S.A. de C.V. (Playas De Rosarito, Mexico) is on the red list of FDA Import Alert 99-08 (Processed human and animal foods: pesticides) for iqf kale, published by FDA on October 29, 2015, 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 99-08 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- Classified NAI (No Action Indicated)
Every FDA record for Fruvemex Mexicali, S.A. de C.V.
2 records, newest first. Each line links to the FDA page it came from.
2019
- InspectionInspection classified NAI (No Action Indicated)Foodborne Biological HazardsSource
2015
- Import alert listingListed on Import Alert 99-08red listIQF KaleSource
Questions about Fruvemex Mexicali, S.A. de C.V.
- Is Fruvemex Mexicali, S.A. de C.V. on an FDA import alert?
- Yes. As of October 27, 2026, Fruvemex Mexicali, S.A. de C.V. is on the red list of FDA Import Alert 99-08, “Processed human and animal foods: pesticides”, for iqf kale; FDA published the listing on October 29, 2015.
- Has FDA refused shipments from Fruvemex Mexicali, S.A. de C.V.?
- No FDA import refusals for Fruvemex Mexicali, S.A. de C.V. appear in FDA's refusal data since October 2016, as of October 27, 2026.
- When was Fruvemex Mexicali, S.A. de C.V. last inspected by FDA?
- FDA's most recent inspection of Fruvemex Mexicali, S.A. de C.V. with a final classification is dated April 10, 2019 and was classified NAI (No Action Indicated).
- What is Fruvemex Mexicali, S.A. de C.V.'s FEI number?
- Fruvemex Mexicali, S.A. de C.V.'s FDA Establishment Identifier (FEI) is 3013125433.
- Can shipments from Fruvemex Mexicali, S.A. de C.V. still enter the U.S.?
- Shipments of iqf kale from Fruvemex Mexicali, S.A. de C.V. can be detained without physical examination under Import Alert 99-08; 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.