Calugi, SRL
FDA import alert and refusal historyCastelfiorentino, ItalyFEI 3013361713
As of October 26, 2026, Calugi, SRL (Castelfiorentino, Italy) is on the red list of FDA Import Alert 99-38 (Low-acid canned/acidified foods: inadequate process control) for all lacf products, published by FDA on June 12, 2026, 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 99-38 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- Classified OAI (Official Action Indicated)
Every FDA record for Calugi, SRL
2 records, newest first. Each line links to the FDA page it came from.
2026
- Import alert listingListed on Import Alert 99-38red listAll LACF productsSource
2025
- InspectionInspection classified OAI (Official Action Indicated)Food Composition, Standards, Labeling and Econ; Foodborne Biological HazardsSource
Questions about Calugi, SRL
- Is Calugi, SRL on an FDA import alert?
- Yes. As of October 26, 2026, Calugi, SRL is on the red list of FDA Import Alert 99-38, “Low-acid canned/acidified foods: inadequate process control”, for all lacf products; FDA published the listing on June 12, 2026.
- Has FDA refused shipments from Calugi, SRL?
- No FDA import refusals for Calugi, SRL appear in FDA's refusal data since October 2016, as of October 26, 2026.
- When was Calugi, SRL last inspected by FDA?
- FDA's most recent inspection of Calugi, SRL with a final classification is dated October 29, 2025 and was classified OAI (Official Action Indicated).
- What is Calugi, SRL's FEI number?
- Calugi, SRL's FDA Establishment Identifier (FEI) is 3013361713.
- Can shipments from Calugi, SRL still enter the U.S.?
- Shipments of all lacf products from Calugi, SRL can be detained without physical examination under Import Alert 99-38; 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.