SKJ & CO
⚠️ Moderate Risk
FEI: 3018375482 • Karachi • PAKISTAN
FEI Number
3018375482
Location
Karachi
Country
PAKISTANAddress
W 2/5 North Western Industrial Zone, Port Qassim, 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
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.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 7/21/2021 | 27YCE03CHUTNEY | 249FILTHY | Division of Southwest Imports (DSWI) |
Frequently Asked Questions
What is SKJ & CO's FDA import refusal history?
SKJ & CO (FEI: 3018375482) has 1 FDA import refusal record(s) in our database, spanning from 7/21/2021 to 7/21/2021.
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. SKJ & CO's FEI number is 3018375482.
What types of violations has SKJ & CO received?
SKJ & CO has been cited for 1 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 SKJ & CO come from?
All FDA import refusal data for SKJ & 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.