Patis France
⚠️ Moderate Risk
FEI: 1000431952 • Rungis CEDEX • FRANCE
FEI Number
1000431952
Location
Rungis CEDEX
Country
FRANCEAddress
46 Rue De Montinery Silic 179, , Rungis CEDEX, , France
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
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).
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.
FILTHY
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the article appears to consist in whole or in part of a filthy, putrid, or decomposed substance or be otherwise unfit for food.
COLOR LBLG
The article appears to contain an artificial coloring and it fails to bear labeling stating that fact.
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.
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).
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 1/17/2012 | 46EG99STABILIZERS AND THICKENERS (FOOD ADDITIVES FOR HUMAN USE) | New York District Office (NYK-DO) | |
| 1/17/2012 | 46EG99STABILIZERS AND THICKENERS (FOOD ADDITIVES FOR HUMAN USE) | 218LIST INGRE | New York District Office (NYK-DO) |
| 1/17/2012 | 46EG99STABILIZERS AND THICKENERS (FOOD ADDITIVES FOR HUMAN USE) | 218LIST INGRE | New York District Office (NYK-DO) |
| 1/17/2012 | 46EG99STABILIZERS AND THICKENERS (FOOD ADDITIVES FOR HUMAN USE) | 218LIST INGRE | New York District Office (NYK-DO) |
| 6/18/2007 | 21LCT03CHERRY, TOPPING OR SYRUP | 274COLOR LBLG | Florida District Office (FLA-DO) |
| 12/14/2006 | 21GET03CHERRY FRUIT (PIT FRUIT) | 11UNSAFE COL | Baltimore District Office (BLT-DO) |
| 11/29/2005 | 21LCT03CHERRY, TOPPING OR SYRUP | 11UNSAFE COL | Florida District Office (FLA-DO) |
| 5/12/2005 | 21LCT03CHERRY, TOPPING OR SYRUP | 11UNSAFE COL | Baltimore District Office (BLT-DO) |
| 12/7/2004 | 23YGT99NUTS OR EDIBLE SEEDS NOT MENTIONED ELSEWHERE, N.E.C. | 249FILTHY | Chicago District Office (CHI-DO) |
| 8/23/2004 | 21LCT03CHERRY, TOPPING OR SYRUP | 11UNSAFE COL | Florida District Office (FLA-DO) |
| 8/23/2004 | 21LCT14PLUM, TOPPING OR SYRUP | 62NEEDS FCE | Florida District Office (FLA-DO) |
| 10/10/2002 | 21GHT03CHERRY FRUIT (PIT FRUIT) | 11UNSAFE COL | Chicago District Office (CHI-DO) |
Frequently Asked Questions
What is Patis France's FDA import refusal history?
Patis France (FEI: 1000431952) has 12 FDA import refusal record(s) in our database, spanning from 10/10/2002 to 1/17/2012.
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. Patis France's FEI number is 1000431952.
What types of violations has Patis France received?
Patis France 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 Patis France come from?
All FDA import refusal data for Patis France 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.