Savini Tartufi SRL
FDA import alert and refusal historyMontanelli Palaia, ItalyFEI 3031487690
Recorded by FDA as SAVINI TARTUFI SRL
As of October 26, 2026, Savini Tartufi SRL is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on October 1, 2026, most often for no scheduled process filed (NO PROCESS).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- Mushrooms and other fungi products, broken or kibbled, n.e.c. · NO PROCESS
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Savini Tartufi SRL
1 record, newest first. Each line links to the FDA page it came from.
2026
- Import refusalRefused, Mushrooms and other fungi products, broken or kibbled, n.e.c.NO PROCESSEntry AMG-0181053-4Source
Refusal charges, in plain English
- NO PROCESS1 refused line
No scheduled process filed
The manufacturer appeared not to have filed a scheduled process with FDA, which 21 CFR Part 108 requires for low-acid canned and acidified foods, so the product is treated as made under insanitary conditions.
Questions about Savini Tartufi SRL
- Is Savini Tartufi SRL on an FDA import alert?
- No listing for Savini Tartufi SRL appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Italy page.
- Has FDA refused shipments from Savini Tartufi SRL?
- Yes. FDA refused 1 shipment line from Savini Tartufi SRL on October 1, 2026. The most recent, on October 1, 2026, was mushrooms and other fungi products, broken or kibbled, n.e.c., charged as NO PROCESS (no scheduled process filed).
- Why did FDA refuse Savini Tartufi SRL's shipments?
- The most frequent charge is NO PROCESS (no scheduled process filed, 1 line).
- What is Savini Tartufi SRL's FEI number?
- Savini Tartufi SRL's FDA Establishment Identifier (FEI) is 3031487690.
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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.