Rafeh Rice Mills
✅ Low Risk
FEI: 3003623098 • Lahore • PAKISTAN
Low Risk
FDA Import Risk Assessment
This firm has a minimal history of FDA import refusals with low-severity violations.
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
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.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 8/9/2002 | 02DGT07RICE, BASMATI, PROCESSED (PACKAGED) | 328USUAL NAME | Detroit District Office (DET-DO) |
Frequently Asked Questions
What is Rafeh Rice Mills's FDA import refusal history?
Rafeh Rice Mills (FEI: 3003623098) has 1 FDA import refusal record(s) in our database, spanning from 8/9/2002 to 8/9/2002.
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. Rafeh Rice Mills's FEI number is 3003623098.
What types of violations has Rafeh Rice Mills received?
Rafeh Rice Mills 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 Rafeh Rice Mills come from?
All FDA import refusal data for Rafeh Rice Mills 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.