Productos Tierra Del Sol S.A. de C.V:
FDA import alert and refusal historyCentro, MexicoFEI 2000004076
As of October 26, 2026, Productos Tierra Del Sol 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 21, 2025, is also listed on Import Alert 12-10 (red list), 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 99-43 · red listIA 12-10 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Productos Tierra Del Sol S.A. de C.V:
2 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 12-10red listCheese/Cheese ProductsSource
Questions about Productos Tierra Del Sol S.A. de C.V:
- Is Productos Tierra Del Sol S.A. de C.V: on an FDA import alert?
- Yes. As of October 26, 2026, Productos Tierra Del Sol 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 21, 2025.
- Has FDA refused shipments from Productos Tierra Del Sol S.A. de C.V:?
- No FDA import refusals for Productos Tierra Del Sol S.A. de C.V: appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Productos Tierra Del Sol S.A. de C.V:'s FEI number?
- Productos Tierra Del Sol S.A. de C.V:'s FDA Establishment Identifier (FEI) is 2000004076.
- Can shipments from Productos Tierra Del Sol S.A. de C.V: still enter the U.S.?
- Shipments of dry hard and san juan queso chincho cheese from Productos Tierra Del Sol 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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