Tigullio S.P.A.
FDA import alert and refusal historyMilan, ItalyFEI 10528
As of October 25, 2026, Tigullio S.P.A. (Milan, Italy) is on the red list of FDA Import Alert 99-38 (Low-acid canned/acidified foods: inadequate process control) for pesto genovese - cream style sauce of sweet basil for pastas; pesto alla genovese cram style paste of sweet basil to season spaghetti, published by FDA on June 3, 2014, 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
- None on record
Every FDA record for Tigullio S.P.A.
1 record, newest first. Each line links to the FDA page it came from.
2014
- Import alert listingListed on Import Alert 99-38red listPesto genovese - cream style sauce of sweet basil for pastas; pesto alla genovese cram style paste of sweet basil to season spaghettiSource
Questions about Tigullio S.P.A.
- Is Tigullio S.P.A. on an FDA import alert?
- Yes. As of October 25, 2026, Tigullio S.P.A. is on the red list of FDA Import Alert 99-38, “Low-acid canned/acidified foods: inadequate process control”, for pesto genovese - cream style sauce of sweet basil for pastas; pesto alla genovese cram style paste of sweet basil to season spaghetti; FDA published the listing on June 3, 2014.
- Has FDA refused shipments from Tigullio S.P.A.?
- No FDA import refusals for Tigullio S.P.A. appear in FDA's refusal data since October 2016, as of October 25, 2026.
- What is Tigullio S.P.A.'s FEI number?
- Tigullio S.P.A.'s FDA Establishment Identifier (FEI) is 10528.
- Can shipments from Tigullio S.P.A. still enter the U.S.?
- Shipments of pesto genovese - cream style sauce of sweet basil for pastas; pesto alla genovese cram style paste of sweet basil to season spaghetti from Tigullio S.P.A. 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.