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Bottarsarda SRL

⚠️ Moderate Risk

FEI: 3005036322 • Quartu Sant'Elena, Cagliari • ITALY

FEI

FEI Number

3005036322

📍

Location

Quartu Sant'Elena, Cagliari

🇮🇹

Country

ITALY
🏢

Address

Via Dante Alighieri 170, , Quartu Sant'Elena, Cagliari, Italy

Moderate Risk

FDA Import Risk Assessment

27.4
LowModerateHighCritical

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

Statistics

2
Total Refusals
4
Unique Violations
3/11/2009
Latest Refusal
5/4/2005
Earliest Refusal

Score Breakdown

Violation Severity
54.0×40%
Refusal Volume
17.7×30%
Recency
0.0×20%
Frequency
5.2×10%
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

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)).

1861×

INSANITARY

The article is subject to refusal of admission pursuant to section 801(a)(3) in that the article appears to have been prepared, packed, or held under insanitary conditions whereby it may have been contaminated with filth, or whereby it may have been rendered injurious to health.

20001×

IMPTRHACCP

The food appears to have been prepared, packed or held under insanitary conditions, or may have become injurious to health, due to the failure of the importer to provide verification of compliance pursuant to 21 CFR 123.12(d).

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.

Refusal History

DateProductViolationsDivision
3/11/2009
16YVT04FISH ROE, FISHERY PRODUCTS, N.E.C.
2000IMPTRHACCP
324NO ENGLISH
Cincinnati District Office (CIN-DO)
5/4/2005
16AVH23MULLET
186INSANITARY
324NO ENGLISH
328USUAL NAME
New Orleans District Office (NOL-DO)

Frequently Asked Questions

What is Bottarsarda SRL's FDA import refusal history?

Bottarsarda SRL (FEI: 3005036322) has 2 FDA import refusal record(s) in our database, spanning from 5/4/2005 to 3/11/2009.

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. Bottarsarda SRL's FEI number is 3005036322.

What types of violations has Bottarsarda SRL received?

Bottarsarda SRL has been cited for 4 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 Bottarsarda SRL come from?

All FDA import refusal data for Bottarsarda 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.