Santa Rita
⚠️ Moderate Risk
FEI: 3011268756 • Porto Salvo • ITALY
FEI Number
3011268756
Location
Porto Salvo
Country
ITALYAddress
Zona Industriale, , Porto Salvo, , 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.
FALSE
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(a)(1 ) of the FD&C Act in that the labeling is false or misleading in any particular.
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.
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.
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)].
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 |
|---|---|---|---|
| 6/30/2015 | 37JCE99SAUCES, N.E.C. | 83NO PROCESS | Baltimore District Office (BLT-DO) |
| 6/30/2015 | 21GCE09OLIVES (PIT FRUIT) | 83NO PROCESS | Baltimore District Office (BLT-DO) |
| 6/11/2015 | 24HCE50TOMATO, DRIED | Baltimore District Office (BLT-DO) | |
| 6/11/2015 | 21GCE09OLIVES (PIT FRUIT) | 83NO PROCESS | Baltimore District Office (BLT-DO) |
| 6/11/2015 | 21ICE09OLIVES (PIT FRUIT PUREES) | 83NO PROCESS | Baltimore District Office (BLT-DO) |
| 3/3/2015 | 37JCE99SAUCES, N.E.C. | 83NO PROCESS | New York District Office (NYK-DO) |
| 3/3/2015 | 37JCE99SAUCES, N.E.C. | 83NO PROCESS | New York District Office (NYK-DO) |
| 3/3/2015 | 37JCE99SAUCES, N.E.C. | 83NO PROCESS | New York District Office (NYK-DO) |
| 3/3/2015 | 21HCE09OLIVES, DRIED OR PASTE | 83NO PROCESS | New York District Office (NYK-DO) |
| 3/3/2015 | 21GCE09OLIVES (PIT FRUIT) | 83NO PROCESS | New York District Office (NYK-DO) |
Frequently Asked Questions
What is Santa Rita's FDA import refusal history?
Santa Rita (FEI: 3011268756) has 10 FDA import refusal record(s) in our database, spanning from 3/3/2015 to 6/30/2015.
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. Santa Rita's FEI number is 3011268756.
What types of violations has Santa Rita received?
Santa Rita 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 Santa Rita come from?
All FDA import refusal data for Santa Rita 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.