Kan Products Ltd
⚠️ Moderate Risk
FEI: 3003320109 • Geneva 15, Geneva • SWITZERLAND
FEI Number
3003320109
Location
Geneva 15, Geneva
Country
SWITZERLANDAddress
Case Postale 1043, , Geneva 15, Geneva, Switzerland
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
NOT LISTED
It appears the drug or device is not included in a list required by Section 510(j), or a notice or other information respecting it was not provided as required by section 510(j) or 510(k).
DIRECTIONS
The article is subject to refusal of admission pursuant to section 801(a)(3) in that it is a device whose label appears to not bear adequate directions for use.
UNAPPROVED
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be a new drug within the meaning of Section 201(p) without an approved New Drug Application (NDA).
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 8/21/2003 | 66VBL99MISCELLANEOUS PATENT MEDICINES, ETC. | Southwest Import District Office (SWI-DO) | |
| 8/21/2003 | 66VBL99MISCELLANEOUS PATENT MEDICINES, ETC. | Southwest Import District Office (SWI-DO) | |
| 8/21/2003 | 64LAJ06BETAMETHASONE DIPROPIONATE (GLUCOCORTICOID) | Southwest Import District Office (SWI-DO) |
Frequently Asked Questions
What is Kan Products Ltd's FDA import refusal history?
Kan Products Ltd (FEI: 3003320109) has 3 FDA import refusal record(s) in our database, spanning from 8/21/2003 to 8/21/2003.
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. Kan Products Ltd's FEI number is 3003320109.
What types of violations has Kan Products Ltd received?
Kan Products Ltd 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 Kan Products Ltd come from?
All FDA import refusal data for Kan Products Ltd 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.