RAUCH Fruchtsaefte GmbH & Co OG
⚠️ Moderate Risk
FEI: 3010112441 • Rankweil, Vorarlberg • AUSTRIA
FEI Number
3010112441
Location
Rankweil, Vorarlberg
Country
AUSTRIAAddress
Langgasse 1, , Rankweil, Vorarlberg, Austria
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 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)).
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.
PESTICIDES
The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to be adulterated because it contains a pesticide chemical, which is in violation of section 402(a)(2)(B). Contains:
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 12/22/2010 | 29YEE99SOFT DRINKS AND WATERS NOT MENTIONED ELSEWHERE, N.E.C. | New York District Office (NYK-DO) | |
| 12/22/2010 | 29YET99SOFT DRINKS AND WATERS NOT MENTIONED ELSEWHERE, N.E.C. | New York District Office (NYK-DO) | |
| 12/22/2010 | 22KCT99OTHER FRUITS AND FRUIT PRODUCTS, OTHER FRUIT JUICES OR CONCENTRATES, N.E.C. | New York District Office (NYK-DO) | |
| 12/22/2010 | 29ACT01SOFT DRINK, BERRY FRUIT FLAVORED, NONCARBONATED | New York District Office (NYK-DO) | |
| 12/22/2010 | 29ACT01SOFT DRINK, BERRY FRUIT FLAVORED, NONCARBONATED | New York District Office (NYK-DO) | |
| 12/22/2010 | 29ACT01SOFT DRINK, BERRY FRUIT FLAVORED, NONCARBONATED | New York District Office (NYK-DO) | |
| 12/22/2010 | 20KCT01CITRON, CITRUS FRUIT JUICES OR CONCENTRATES | New York District Office (NYK-DO) | |
| 11/17/2004 | 20DGO13RASPBERRY, RED, BERRY JUICE OR CONCENTRATES | 2920PESTICIDES | Seattle District Office (SEA-DO) |
Frequently Asked Questions
What is RAUCH Fruchtsaefte GmbH & Co OG's FDA import refusal history?
RAUCH Fruchtsaefte GmbH & Co OG (FEI: 3010112441) has 8 FDA import refusal record(s) in our database, spanning from 11/17/2004 to 12/22/2010.
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. RAUCH Fruchtsaefte GmbH & Co OG's FEI number is 3010112441.
What types of violations has RAUCH Fruchtsaefte GmbH & Co OG received?
RAUCH Fruchtsaefte GmbH & Co OG has been cited for 3 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 RAUCH Fruchtsaefte GmbH & Co OG come from?
All FDA import refusal data for RAUCH Fruchtsaefte GmbH & Co OG 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.