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Ciro Velleca S.R.L.

⚠️ Moderate Risk

FEI: 3004306738 • Sant'Anastasia, Naples • ITALY

FEI

FEI Number

3004306738

📍

Location

Sant'Anastasia, Naples

🇮🇹

Country

ITALY
🏢

Address

Via Pomigliano N. 25, , Sant'Anastasia, Naples, Italy

Moderate Risk

FDA Import Risk Assessment

29.2
LowModerateHighCritical

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

Statistics

4
Total Refusals
12
Unique Violations
3/31/2015
Latest Refusal
11/16/2012
Earliest Refusal

Score Breakdown

Violation Severity
49.4×40%
Refusal Volume
25.9×30%
Recency
0.0×20%
Frequency
16.9×10%
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

3282×

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.

2182×

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.

33002×

ALLERGEN

the label fails to declare all major food allergens present in the product, as required by section 403(w)(1).

3202×

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.

3212×

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.

3242×

NO ENGLISH

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(f) of the FD&C Act in that any word, statement, or other information required by or under the authority of the FD&C Act to appear on the label or labeling is not prominently placed thereon with such conspicuousness (as compared with other words, statements, designs, or devices, in the labeling) and in such terms as to render it likely to be read and understood by the ordinary individual under customary terms of purchase and use (for example, label contains information in two or more languages but fails to repeat all required information in both languages in accordance with 21 CFR 101.15(c)(2), or label fails to include all required information in English in accordance with 21 CFR 101.15(c)(1), except in the case of articles distributed solely in the Commonwealth of Puerto Rico or in a Territory where the predominant language is one other than English)).

751×

UNAPPROVED

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be a new drug within the meaning of Section 201(p) without an approved New Drug Application (NDA).

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).

32801×

FRNMFGREG

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to be misbranded as defined in section 502(o) of the FD&C Act. It appears that it was manufactured, prepared, propagated, compounded, or processed in an establishment not duly registered under section 510 of the Act.

33201×

TRANSFAT

The product is misbranded under Section 403(q) because the nutrition label does not provide all of the information required by 21 CFR 101.9(c); specifically, the label does not bear the amount of trans fat [21 CFR 101.9(c)(2)(ii)].

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.

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).

Refusal History

DateProductViolationsDivision
3/31/2015
65RAR18SODIUM BICARBONATE (REPLENISHER)
118NOT LISTED
3280FRNMFGREG
75UNAPPROVED
Division of Northeast Imports (DNEI)
12/24/2013
23EGT06FILBERT, HAZELNUT, SPREAD
218LIST INGRE
320LACKS FIRM
321LACKS N/C
324NO ENGLISH
328USUAL NAME
3300ALLERGEN
482NUTRIT LBL
Division of Northeast Imports (DNEI)
12/24/2013
23EGT06FILBERT, HAZELNUT, SPREAD
218LIST INGRE
320LACKS FIRM
321LACKS N/C
324NO ENGLISH
328USUAL NAME
3300ALLERGEN
Division of Northeast Imports (DNEI)
11/16/2012
21GCT09OLIVES (PIT FRUIT)
11UNSAFE COL
3320TRANSFAT
New York District Office (NYK-DO)

Frequently Asked Questions

What is Ciro Velleca S.R.L.'s FDA import refusal history?

Ciro Velleca S.R.L. (FEI: 3004306738) has 4 FDA import refusal record(s) in our database, spanning from 11/16/2012 to 3/31/2015.

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. Ciro Velleca S.R.L.'s FEI number is 3004306738.

What types of violations has Ciro Velleca S.R.L. received?

Ciro Velleca S.R.L. has been cited for 12 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 Ciro Velleca S.R.L. come from?

All FDA import refusal data for Ciro Velleca S.R.L. 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.