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Segafredo Zanetti S.p.A.

⚠️ Moderate Risk

FEI: 3004321529 • Pianoro, Bologna • ITALY

FEI

FEI Number

3004321529

📍

Location

Pianoro, Bologna

🇮🇹

Country

ITALY
🏢

Address

Via Giacomo Puccini 1, , Pianoro, Bologna, Italy

Moderate Risk

FDA Import Risk Assessment

26.6
LowModerateHighCritical

This firm has a moderate history of FDA import refusals. Some attention may be warranted.

Statistics

2
Total Refusals
6
Unique Violations
8/20/2012
Latest Refusal
12/8/2011
Earliest Refusal

Score Breakdown

Violation Severity
48.3×40%
Refusal Volume
17.7×30%
Recency
0.0×20%
Frequency
20.0×10%
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

111×

UNSAFE COL

The article appears to be, or to bear or contain a color additive which is unsafe within the meaning of Section 721(a).

1181×

NOT LISTED

It appears the drug or device is not included in a list required by Section 510(j), or a notice or other information respecting it was not provided as required by section 510(j) or 510(k).

2181×

LIST INGRE

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)(2) of the FD&C Act in that it is fabricated from two or more ingredients and the label fails to bear the common or usual name of each such ingredient and/or the article purports to be a beverage containing vegetable or fruit juice, but does not bear a statement with appropriate prominence on the information panel of the total percentage of such fruit or vegetable juice contained in the food.

3211×

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.

3281×

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.

4821×

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.

Refusal History

DateProductViolationsDivision
8/20/2012
53YY01HAIR BRUSH (OTHER COSMETIC AND COSMETIC PRODUCTS)
118NOT LISTED
Florida District Office (FLA-DO)
12/8/2011
34FFT01CHOCOLATE CANDY BAR, WITHOUT NUTS AND FRUIT
11UNSAFE COL
218LIST INGRE
321LACKS N/C
328USUAL NAME
482NUTRIT LBL
Baltimore District Office (BLT-DO)

Frequently Asked Questions

What is Segafredo Zanetti S.p.A.'s FDA import refusal history?

Segafredo Zanetti S.p.A. (FEI: 3004321529) has 2 FDA import refusal record(s) in our database, spanning from 12/8/2011 to 8/20/2012.

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. Segafredo Zanetti S.p.A.'s FEI number is 3004321529.

What types of violations has Segafredo Zanetti S.p.A. received?

Segafredo Zanetti S.p.A. has been cited for 6 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 Segafredo Zanetti S.p.A. come from?

All FDA import refusal data for Segafredo Zanetti S.p.A. 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.