Expo India
⚠️ Moderate Risk
FEI: 3000256838 • Moradabad, UP • INDIA
FEI Number
3000256838
Location
Moradabad, UP
Country
INDIAAddress
Unknown Street, , Moradabad, UP, India
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
UNSAFE ADD
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to bear or contain an unsafe food additive within the meaning of section 409.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 3/29/2013 | 52AID38SPOONS (FOODWARE, COOKWARE & TABLEWARE) | 238UNSAFE ADD | San Francisco District Office (SAN-DO) |
Frequently Asked Questions
What is Expo India's FDA import refusal history?
Expo India (FEI: 3000256838) has 1 FDA import refusal record(s) in our database, spanning from 3/29/2013 to 3/29/2013.
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. Expo India's FEI number is 3000256838.
What types of violations has Expo India received?
Expo India 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 Expo India come from?
All FDA import refusal data for Expo India 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.