Tartuflanghe SRL
⚠️ Moderate Risk
FEI: 3003015180 • Piobesi D'Alba, Cuneo • ITALY
FEI Number
3003015180
Location
Piobesi D'Alba, Cuneo
Country
ITALYAddress
Regione Catena Rossa 7, , Piobesi D'Alba, Cuneo, Italy
Moderate Risk
FDA Import Risk Assessment
This firm has a moderate history of FDA import refusals. Some attention may be warranted.
Statistics
Score Breakdown
How is this score calculated?
Proprietary Algorithm
- 40% Violation Severity — AI-assessed (1-10)
- 30% Refusal Volume — Logarithmic scale
- 20% Recency — Decays over 5 years
- 10% Frequency — Refusals per year
© ImportRefusal.com Original Analysis
Violation Summary
NO PROCESS
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the manufacturer's failure to file a scheduled process demonstrates that the product is not being manufactured under the mandatory provisions of 21 CFR Part 108 and therefore appears to have been manufactured, processed, or packed, under insanitary conditions whereby it may have been rendered injurious to health.
NEEDS FCE
It appears the manufacturer is not registered as a low acid canned food or acidified food manufacturer pursuant to 21 CFR 108.25(c)(1) or 108.35(c)(1).
LACKS N/C
The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of Section 403(e)(2) of the FD&C Act in that the food is in package form and the label fails to bear an accurate statement of the quantity of the contents in terms of weight, measure, or numerical count in accordance with Section 403(e)(2) of the FD&C Act.
USUAL NAME
The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of Section 403(i)(1) of the FD&C Act in that the label fails to bear the common or usual name of the food, if any there be.
LACKS FIRM
The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of Section 403(e)(1) of the FD&C Act in that the food is in package form and the label fails to bear the name and place of business of the manufacturer, packer, or distributor.
NUTRIT LBL
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be misbranded in that the label or labeling fails to bear the required nutrition information.
DIETARYLBL
The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it is a dietary supplement that appears to be misbranded within the meaning of Section 403(s)(2)(B) of the FD&C Act in that the label or labeling fails to identify the product by using the term "dietary supplement", which term may be modified with the name of such an ingredient.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 4/26/2012 | 25QCE02TRUFFLE, PIECES AND STEMS, SLICED | New Orleans District Office (NOL-DO) | |
| 4/26/2012 | 25SCE02TRUFFLE, FUNGI PRODUCTS, N.E.C. | New Orleans District Office (NOL-DO) | |
| 8/13/2008 | 25PCE02TRUFFLE, WHOLE (BUTTON) (FUNGI) | 83NO PROCESS | New Orleans District Office (NOL-DO) |
| 3/14/2005 | 25QCT02TRUFFLE, PIECES AND STEMS, SLICED | 83NO PROCESS | New York District Office (NYK-DO) |
| 2/10/2004 | 25QCE02TRUFFLE, PIECES AND STEMS, SLICED | New York District Office (NYK-DO) | |
| 12/19/2002 | 25SGT02TRUFFLE, FUNGI PRODUCTS, N.E.C. | Florida District Office (FLA-DO) |
Frequently Asked Questions
What is Tartuflanghe SRL's FDA import refusal history?
Tartuflanghe SRL (FEI: 3003015180) has 6 FDA import refusal record(s) in our database, spanning from 12/19/2002 to 4/26/2012.
What is an FEI number?
FEI stands for Firm Establishment Identifier. It's a unique number assigned by the FDA to identify establishments that manufacture, process, pack, or hold food, drugs, medical devices, or other FDA-regulated products. Tartuflanghe SRL's FEI number is 3003015180.
What types of violations has Tartuflanghe SRL received?
Tartuflanghe SRL has been cited for 7 different violation type(s). Common FDA violations include adulteration (unsafe or unsanitary products), misbranding (incorrect or misleading labels), and regulatory non-compliance.
Where does this information about Tartuflanghe SRL come from?
All FDA import refusal data for Tartuflanghe SRL is sourced from the official FDA Data Dashboard (datadashboard.fda.gov), a public government database maintained by the U.S. Food and Drug Administration.
Data sourced from the FDA Data Dashboard, a public database maintained by the U.S. Food and Drug Administration.