Comercializadora Mexicana De Legumbres SA de CV (COMELESA)
FDA import alert and refusal historyAcatzingo, MexicoFEI 3003411315
As of October 27, 2026, Comercializadora Mexicana De Legumbres SA de CV (COMELESA) (Acatzingo, Mexico) is on the red list of FDA Import Alert 99-08 (Processed human and animal foods: pesticides) for frozen hawthorne apple (tejocote), published by FDA on May 18, 2011, 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
- None on record
Every FDA record for Comercializadora Mexicana De Legumbres SA de CV (COMELESA)
1 record, newest first. Each line links to the FDA page it came from.
2011
- Import alert listingListed on Import Alert 99-08red listFrozen Hawthorne Apple (Tejocote)Source
Questions about Comercializadora Mexicana De Legumbres SA de CV (COMELESA)
- Is Comercializadora Mexicana De Legumbres SA de CV (COMELESA) on an FDA import alert?
- Yes. As of October 27, 2026, Comercializadora Mexicana De Legumbres SA de CV (COMELESA) is on the red list of FDA Import Alert 99-08, “Processed human and animal foods: pesticides”, for frozen hawthorne apple (tejocote); FDA published the listing on May 18, 2011.
- Has FDA refused shipments from Comercializadora Mexicana De Legumbres SA de CV (COMELESA)?
- No FDA import refusals for Comercializadora Mexicana De Legumbres SA de CV (COMELESA) appear in FDA's refusal data since October 2016, as of October 27, 2026.
- What is Comercializadora Mexicana De Legumbres SA de CV (COMELESA)'s FEI number?
- Comercializadora Mexicana De Legumbres SA de CV (COMELESA)'s FDA Establishment Identifier (FEI) is 3003411315.
- Can shipments from Comercializadora Mexicana De Legumbres SA de CV (COMELESA) still enter the U.S.?
- Shipments of frozen hawthorne apple (tejocote) from Comercializadora Mexicana De Legumbres SA de CV (COMELESA) 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.