S. Amden & Co.
⚠️ Moderate Risk
FEI: 3001657707 • Karachi • PAKISTAN
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
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.
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).
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.
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.
LABELING
The article appears in violation of FPLA because of its placement, form and/or contents statement.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 2/12/2013 | 28MCT99IMITATION FLAVOR, N.E.C. | Southwest Import District Office (SWI-DO) | |
| 2/12/2013 | 28MCT99IMITATION FLAVOR, N.E.C. | Southwest Import District Office (SWI-DO) | |
| 10/5/2011 | 28CCT39ROSE (ATTAR OF ROSES), NATURAL EXTRACT OR FLAVOR (SPICE) | New York District Office (NYK-DO) | |
| 10/26/2004 | 31ACY99COFFEE, N.E.C. | Division of Southwest Imports (DSWI) |
Frequently Asked Questions
What is S. Amden & Co.'s FDA import refusal history?
S. Amden & Co. (FEI: 3001657707) has 4 FDA import refusal record(s) in our database, spanning from 10/26/2004 to 2/12/2013.
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. S. Amden & Co.'s FEI number is 3001657707.
What types of violations has S. Amden & Co. received?
S. Amden & Co. has been cited for 5 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 S. Amden & Co. come from?
All FDA import refusal data for S. Amden & Co. 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.