Smeralda
⚠️ Moderate Risk
FEI: 3003861133 • Cagliari, Cagliari • ITALY
FEI Number
3003861133
Location
Cagliari, Cagliari
Country
ITALYAddress
Via Dell' Industria 13, , Cagliari, Cagliari, 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
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.
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.
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)).
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.
INSANITARY
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to have been prepared, packed, or held under insanitary conditions whereby it may have become contaminated with filth, or whereby it may have been rendered injurious to health.
MFR INSAN
The article is subject to refusal of admission pursuant to section 801(a)(1) in that the article appears to have been manufactured, processed, or packed under insanitary conditions.
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)].
POISONOUS
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to bear or contain a poisonous or deleterious substance which may render the article injurious to health. Contains:
LABELING
The article appears in violation of FPLA because of its placement, form and/or contents statement.
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).
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 7/16/2009 | 16AVH23MULLET | Cincinnati District Office (CIN-DO) | |
| 6/1/2007 | 16AEE45TUNA (ALBACORE, YELLOWFIN, BLUEFIN, SKIPJACK, ETC.) | Southwest Import District Office (SWI-DO) | |
| 6/1/2007 | 16AEO45TUNA (ALBACORE, YELLOWFIN, BLUEFIN, SKIPJACK, ETC.) | Southwest Import District Office (SWI-DO) | |
| 6/1/2007 | 16AEE45TUNA (ALBACORE, YELLOWFIN, BLUEFIN, SKIPJACK, ETC.) | Southwest Import District Office (SWI-DO) | |
| 6/1/2007 | 33AVE13ROCK CANDY, HARD, WITH NUTS OR NUT PRODUCTS (NOT COCONUT) (WITHOUT CHOCOLATE) | Southwest Import District Office (SWI-DO) | |
| 6/1/2007 | 33AVE13ROCK CANDY, HARD, WITH NUTS OR NUT PRODUCTS (NOT COCONUT) (WITHOUT CHOCOLATE) | Southwest Import District Office (SWI-DO) | |
| 6/1/2007 | 16ACH23MULLET | Southwest Import District Office (SWI-DO) | |
| 6/1/2007 | 16ACH23MULLET | Southwest Import District Office (SWI-DO) | |
| 6/1/2007 | 16AEE45TUNA (ALBACORE, YELLOWFIN, BLUEFIN, SKIPJACK, ETC.) | Southwest Import District Office (SWI-DO) | |
| 6/1/2007 | 16SVH42SWORDFISH, COLD SMOKED, FISH | 251POISONOUS | Southwest Import District Office (SWI-DO) |
| 6/1/2007 | 16SVH42SWORDFISH, COLD SMOKED, FISH | 251POISONOUS | Southwest Import District Office (SWI-DO) |
| 2/20/2007 | 16MEO11SEA URCHIN, OTHER AQUATIC SPECIES | San Francisco District Office (SAN-DO) | |
| 2/20/2007 | 16ACS45TUNA (ALBACORE, YELLOWFIN, BLUEFIN, SKIPJACK, ETC.) | San Francisco District Office (SAN-DO) | |
| 2/20/2007 | 16AEO45TUNA (ALBACORE, YELLOWFIN, BLUEFIN, SKIPJACK, ETC.) | San Francisco District Office (SAN-DO) | |
| 11/7/2005 | 16AVC45TUNA (ALBACORE, YELLOWFIN, BLUEFIN, SKIPJACK, ETC.) | 308MFR INSAN | Cincinnati District Office (CIN-DO) |
| 11/7/2005 | 16AVC23MULLET | 308MFR INSAN | Cincinnati District Office (CIN-DO) |
| 10/24/2005 | 16AVH23MULLET | Cincinnati District Office (CIN-DO) | |
| 10/24/2005 | 16AVH45TUNA (ALBACORE, YELLOWFIN, BLUEFIN, SKIPJACK, ETC.) | Cincinnati District Office (CIN-DO) |
Frequently Asked Questions
What is Smeralda's FDA import refusal history?
Smeralda (FEI: 3003861133) has 18 FDA import refusal record(s) in our database, spanning from 10/24/2005 to 7/16/2009.
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. Smeralda's FEI number is 3003861133.
What types of violations has Smeralda received?
Smeralda has been cited for 11 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 Smeralda come from?
All FDA import refusal data for Smeralda 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.