Caseificio Voglia di latte srl
FDA import alert and refusal historyBisceglie, ItalyFEI 2000013641
As of October 26, 2026, Caseificio Voglia di latte srl (Bisceglie, Italy) is on the red list of FDA Import Alert 12-10 (Cheese: microbiological contamination) for cheese, semisoft; soft, semi-soft cheese made from cow's milk (includes feta type cheese), 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 Caseificio Voglia di latte srl
1 record, newest first. Each line links to the FDA page it came from.
2009
- Import alert listingListed on Import Alert 12-10red listCheese, Semisoft; Soft, semi-soft cheese made from cow's milk (includes feta type cheese)Source
Questions about Caseificio Voglia di latte srl
- Is Caseificio Voglia di latte srl on an FDA import alert?
- Yes. As of October 26, 2026, Caseificio Voglia di latte srl is on the red list of FDA Import Alert 12-10, “Cheese: microbiological contamination”, for cheese, semisoft; soft, semi-soft cheese made from cow's milk (includes feta type cheese); FDA published the listing on September 18, 2009.
- Has FDA refused shipments from Caseificio Voglia di latte srl?
- No FDA import refusals for Caseificio Voglia di latte srl appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Caseificio Voglia di latte srl's FEI number?
- Caseificio Voglia di latte srl's FDA Establishment Identifier (FEI) is 2000013641.
- Can shipments from Caseificio Voglia di latte srl still enter the U.S.?
- Shipments of cheese, semisoft; soft, semi-soft cheese made from cow's milk (includes feta type cheese) from Caseificio Voglia di latte srl 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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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.