Cinquina International
⚠️ Moderate Risk
FEI: 3013136723 • Lanciano, Chieti • ITALY
FEI Number
3013136723
Location
Lanciano, Chieti
Country
ITALYAddress
Loc. Cerratina 77/ I, , Lanciano, Chieti, 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).
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.
LABELING
The article appears in violation of FPLA because of its placement, form and/or contents statement.
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
| Date | Product | Violations | Division |
|---|---|---|---|
| 8/1/2017 | 21GCE11OLIVES, GREEN, (PIT FRUIT) | 218LIST INGRE | Division of Northeast Imports (DNEI) |
| 8/1/2017 | 21GCE11OLIVES, GREEN, (PIT FRUIT) | 218LIST INGRE | Division of Northeast Imports (DNEI) |
| 8/1/2017 | 21GCE11OLIVES, GREEN, (PIT FRUIT) | 218LIST INGRE | Division of Northeast Imports (DNEI) |
| 3/18/2013 | 21GCP09OLIVES (PIT FRUIT) | 83NO PROCESS | San Francisco District Office (SAN-DO) |
| 5/30/2012 | 24FEI50TOMATOES (FRUIT USED AS VEGETABLE) | Seattle District Office (SEA-DO) | |
| 6/26/2007 | 21GCP09OLIVES (PIT FRUIT) | 83NO PROCESS | New York District Office (NYK-DO) |
| 3/19/2007 | 17CCE99COMBINATION PREPARED MEAT PRODUCTS, N.E.C. | San Francisco District Office (SAN-DO) | |
| 3/19/2007 | 25ECE99MIXED VEGETABLES, N.E.C. | San Francisco District Office (SAN-DO) | |
| 3/19/2007 | 21ICE09OLIVES (PIT FRUIT PUREES) | San Francisco District Office (SAN-DO) | |
| 3/19/2007 | 21GYT09OLIVES (PIT FRUIT) | San Francisco District Office (SAN-DO) | |
| 3/19/2007 | 21ICB09OLIVES (PIT FRUIT PUREES) | San Francisco District Office (SAN-DO) | |
| 1/17/2006 | 24HCE04PIMIENTO PEPPER, DRIED OR PASTE | New York District Office (NYK-DO) | |
| 4/4/2005 | 21GVE09OLIVES (PIT FRUIT) | 83NO PROCESS | Chicago District Office (CHI-DO) |
| 4/1/2005 | 21GVE09OLIVES (PIT FRUIT) | 83NO PROCESS | Chicago District Office (CHI-DO) |
| 4/1/2005 | 21GVE09OLIVES (PIT FRUIT) | 83NO PROCESS | Chicago District Office (CHI-DO) |
| 4/1/2005 | 24HCE50TOMATO, DRIED | 83NO PROCESS | Chicago District Office (CHI-DO) |
| 4/1/2005 | 21GCE09OLIVES (PIT FRUIT) | 83NO PROCESS | Chicago District Office (CHI-DO) |
| 4/1/2005 | 21GCE09OLIVES (PIT FRUIT) | 83NO PROCESS | Chicago District Office (CHI-DO) |
Frequently Asked Questions
What is Cinquina International's FDA import refusal history?
Cinquina International (FEI: 3013136723) has 18 FDA import refusal record(s) in our database, spanning from 4/1/2005 to 8/1/2017.
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. Cinquina International's FEI number is 3013136723.
What types of violations has Cinquina International received?
Cinquina International has been cited for 5 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 Cinquina International come from?
All FDA import refusal data for Cinquina International 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.