Operadora De Lacteos Santa Julia, Sde R.L. Mi.
FDA import alert and refusal historyDelicias, MexicoFEI 3003603873
As of October 26, 2026, Operadora De Lacteos Santa Julia, Sde R.L. Mi. (Delicias, Mexico) is on the red list of FDA Import Alert 12-10 (Cheese: microbiological contamination) for cheese, hispanic/latino/mexican style, all varieties, including queso, published by FDA on September 18, 2009, 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 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 Operadora De Lacteos Santa Julia, Sde R.L. Mi.
1 record, newest first. Each line links to the FDA page it came from.
2009
- Import alert listingListed on Import Alert 12-10red listCheese, Hispanic/Latino/Mexican Style, all varieties, including quesoSource
Questions about Operadora De Lacteos Santa Julia, Sde R.L. Mi.
- Is Operadora De Lacteos Santa Julia, Sde R.L. Mi. on an FDA import alert?
- Yes. As of October 26, 2026, Operadora De Lacteos Santa Julia, Sde R.L. Mi. is on the red list of FDA Import Alert 12-10, “Cheese: microbiological contamination”, for cheese, hispanic/latino/mexican style, all varieties, including queso; FDA published the listing on September 18, 2009.
- Has FDA refused shipments from Operadora De Lacteos Santa Julia, Sde R.L. Mi.?
- No FDA import refusals for Operadora De Lacteos Santa Julia, Sde R.L. Mi. appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Operadora De Lacteos Santa Julia, Sde R.L. Mi.'s FEI number?
- Operadora De Lacteos Santa Julia, Sde R.L. Mi.'s FDA Establishment Identifier (FEI) is 3003603873.
- Can shipments from Operadora De Lacteos Santa Julia, Sde R.L. Mi. still enter the U.S.?
- Shipments of cheese, hispanic/latino/mexican style, all varieties, including queso from Operadora De Lacteos Santa Julia, Sde R.L. Mi. can be detained without physical examination under Import Alert 12-10; 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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