chilemex s.a. de c.v.
FDA import alert and refusal historyCentro, MexicoFEI 3004404719
As of October 26, 2026, chilemex s.a. de c.v. (Centro, Mexico) is on the red list of FDA Import Alert 99-43 (Ready-to-eat foods: insanitary conditions) for dry hard and san juan queso chincho cheese, published by FDA on August 26, 2025, is also listed on Import Alert 12-10 (red list) and Import Alert 16-81 (red list) and Import Alert 45-02 (red list), and has no FDA import refusals recorded since October 2016.
Data from FDA public records, last checked . Request a correction
Current status
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for chilemex s.a. de c.v.
4 records, newest first. Each line links to the FDA page it came from.
2025
- Import alert listingListed on Import Alert 99-43red listDry Hard and San Juan Queso Chincho cheeseSource
2009
- Import alert listingListed on Import Alert 45-02red listPepper, Hot, Dried or Paste; hard candy grageas; Cake Decoration (without Chocolate)Source
- Import alert listingListed on Import Alert 16-81red listFish, N.E.C.; ShrimpSource
- Import alert listingListed on Import Alert 12-10red listCheese/Cheese ProductsSource
Questions about chilemex s.a. de c.v.
- Is chilemex s.a. de c.v. on an FDA import alert?
- Yes. As of October 26, 2026, chilemex s.a. de c.v. is on the red list of FDA Import Alert 99-43, “Ready-to-eat foods: insanitary conditions”, for dry hard and san juan queso chincho cheese; FDA published the listing on August 26, 2025.
- Has FDA refused shipments from chilemex s.a. de c.v.?
- No FDA import refusals for chilemex s.a. de c.v. appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is chilemex s.a. de c.v.'s FEI number?
- chilemex s.a. de c.v.'s FDA Establishment Identifier (FEI) is 3004404719.
- Can shipments from chilemex s.a. de c.v. still enter the U.S.?
- Shipments of dry hard and san juan queso chincho cheese from chilemex s.a. de c.v. can be detained without physical examination under Import Alert 99-43; 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.