CLIN Coop Produttori Latte Indenne Della Provincia Di Novara
FDA import alert and refusal historyCampriano, ItalyFEI 1000134220
As of October 26, 2026, CLIN Coop Produttori Latte Indenne Della Provincia Di Novara (Campriano, Italy) is on the red list of FDA Import Alert 12-10 (Cheese: microbiological contamination) for cheese, gorgonzola, 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 CLIN Coop Produttori Latte Indenne Della Provincia Di Novara
1 record, newest first. Each line links to the FDA page it came from.
2009
- Import alert listingListed on Import Alert 12-10red listCheese, GorgonzolaSource
Questions about CLIN Coop Produttori Latte Indenne Della Provincia Di Novara
- Is CLIN Coop Produttori Latte Indenne Della Provincia Di Novara on an FDA import alert?
- Yes. As of October 26, 2026, CLIN Coop Produttori Latte Indenne Della Provincia Di Novara is on the red list of FDA Import Alert 12-10, “Cheese: microbiological contamination”, for cheese, gorgonzola; FDA published the listing on September 18, 2009.
- Has FDA refused shipments from CLIN Coop Produttori Latte Indenne Della Provincia Di Novara?
- No FDA import refusals for CLIN Coop Produttori Latte Indenne Della Provincia Di Novara appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is CLIN Coop Produttori Latte Indenne Della Provincia Di Novara's FEI number?
- CLIN Coop Produttori Latte Indenne Della Provincia Di Novara's FDA Establishment Identifier (FEI) is 1000134220.
- Can shipments from CLIN Coop Produttori Latte Indenne Della Provincia Di Novara still enter the U.S.?
- Shipments of cheese, gorgonzola from CLIN Coop Produttori Latte Indenne Della Provincia Di Novara 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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