Lacteos Don Chente S.A. de C.V.
FDA import alert and refusal historyCiudad Juarez, MexicoFEI 3004965515
As of October 26, 2026, Lacteos Don Chente S.A. de C.V. (Ciudad Juarez, Mexico) is on the red list of FDA Import Alert 99-43 (Ready-to-eat foods: insanitary conditions) for asadero cheese ball, published by FDA on August 25, 2025, 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 list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- Classified VAI (Voluntary Action Indicated)
Every FDA record for Lacteos Don Chente 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 listAsadero cheese ballSource
2009
- InspectionInspection classified VAI (Voluntary Action Indicated)Foodborne Biological HazardsSource
Questions about Lacteos Don Chente S.A. de C.V.
- Is Lacteos Don Chente S.A. de C.V. on an FDA import alert?
- Yes. As of October 26, 2026, Lacteos Don Chente S.A. de C.V. is on the red list of FDA Import Alert 99-43, “Ready-to-eat foods: insanitary conditions”, for asadero cheese ball; FDA published the listing on August 25, 2025.
- Has FDA refused shipments from Lacteos Don Chente S.A. de C.V.?
- No FDA import refusals for Lacteos Don Chente S.A. de C.V. appear in FDA's refusal data since October 2016, as of October 26, 2026.
- When was Lacteos Don Chente S.A. de C.V. last inspected by FDA?
- FDA's most recent inspection of Lacteos Don Chente S.A. de C.V. with a final classification is dated September 25, 2009 and was classified VAI (Voluntary Action Indicated).
- What is Lacteos Don Chente S.A. de C.V.'s FEI number?
- Lacteos Don Chente S.A. de C.V.'s FDA Establishment Identifier (FEI) is 3004965515.
- Can shipments from Lacteos Don Chente S.A. de C.V. still enter the U.S.?
- Shipments of asadero cheese ball from Lacteos Don Chente 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.