Alfarid Corporation
⚠️ Moderate Risk
FEI: 3008178318 • Karachi • PAKISTAN
FEI Number
3008178318
Location
Karachi
Country
PAKISTANAddress
Fourth Floor 20-C Mainkhayaban-E Shahbaz, , 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.
LACKS FIRM
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(e)(1) of the FD&C Act in that the food is in package form and the label fails to bear the name and place of business of the manufacturer, packer, or distributor.
TRANSFAT
The product is misbranded under Section 403(q) because the nutrition label does not provide all of the information required by 21 CFR 101.9(c); specifically, the label does not bear the amount of trans fat [21 CFR 101.9(c)(2)(ii)].
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.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 9/9/2010 | 02DAB07RICE, BASMATI, PROCESSED (PACKAGED) | Detroit District Office (DET-DO) | |
| 9/9/2010 | 02DAB07RICE, BASMATI, PROCESSED (PACKAGED) | Detroit District Office (DET-DO) | |
| 9/9/2010 | 02DAB07RICE, BASMATI, PROCESSED (PACKAGED) | Detroit District Office (DET-DO) |
Frequently Asked Questions
What is Alfarid Corporation's FDA import refusal history?
Alfarid Corporation (FEI: 3008178318) has 3 FDA import refusal record(s) in our database, spanning from 9/9/2010 to 9/9/2010.
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. Alfarid Corporation's FEI number is 3008178318.
What types of violations has Alfarid Corporation received?
Alfarid Corporation has been cited for 4 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 Alfarid Corporation come from?
All FDA import refusal data for Alfarid Corporation 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.