Firma Franz Kastner Gmbh
⚠️ Moderate Risk
FEI: 3003795523 • Bad Leonfelden • GERMANY
FEI Number
3003795523
Location
Bad Leonfelden
Country
GERMANYAddress
Linzer Strasse 25, , Bad Leonfelden, , Germany
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.
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).
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 7/15/2003 | 36CYT99HONEY, N.E.C. | 482NUTRIT LBL | Atlanta District Office (ATL-DO) |
| 7/15/2003 | 34EYT02CHOCOLATE CANDY PIECES, WITH FRUIT AND FRUIT PRODUCTS | 482NUTRIT LBL | Atlanta District Office (ATL-DO) |
| 7/15/2003 | 22LCN99OTHER FRUIT AND FRUIT PRODUCTS, TOPPING OR SYRUP, N.E.C. | 11UNSAFE COL | Atlanta District Office (ATL-DO) |
Frequently Asked Questions
What is Firma Franz Kastner Gmbh's FDA import refusal history?
Firma Franz Kastner Gmbh (FEI: 3003795523) has 3 FDA import refusal record(s) in our database, spanning from 7/15/2003 to 7/15/2003.
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. Firma Franz Kastner Gmbh's FEI number is 3003795523.
What types of violations has Firma Franz Kastner Gmbh received?
Firma Franz Kastner Gmbh has been cited for 2 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 Firma Franz Kastner Gmbh come from?
All FDA import refusal data for Firma Franz Kastner Gmbh 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.