ITC LIMITED
⚠️ High Risk
FEI: 3006292098 • Guntur, Andhra Pradesh • INDIA
FEI Number
3006292098
Location
Guntur, Andhra Pradesh
Country
INDIAAddress
P B 317 G.T. Road, , Guntur, Andhra Pradesh, India
High Risk
FDA Import Risk Assessment
This firm has a significant history of FDA import refusals with notable 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
PESTICIDES
The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to be adulterated because it contains a pesticide chemical, which is in violation of section 402(a)(2)(B). Contains:
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.
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.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 3/23/2011 | 28AGH08CAPSICUMS (CAYENNE CHILI, HOT PEPPERS), WHOLE (SPICE) | 2920PESTICIDES | Los Angeles District Office (LOS-DO) |
| 3/15/2011 | 28AGT08CAPSICUMS (CAYENNE CHILI, HOT PEPPERS), WHOLE (SPICE) | 2920PESTICIDES | New York District Office (NYK-DO) |
| 3/10/2011 | 28AAH08CAPSICUMS (CAYENNE CHILI, HOT PEPPERS), WHOLE (SPICE) | 2920PESTICIDES | Baltimore District Office (BLT-DO) |
| 3/10/2011 | 28AAH08CAPSICUMS (CAYENNE CHILI, HOT PEPPERS), WHOLE (SPICE) | 2920PESTICIDES | Baltimore District Office (BLT-DO) |
| 2/28/2011 | 28AAH08CAPSICUMS (CAYENNE CHILI, HOT PEPPERS), WHOLE (SPICE) | 2920PESTICIDES | San Francisco District Office (SAN-DO) |
| 2/28/2011 | 28AAH08CAPSICUMS (CAYENNE CHILI, HOT PEPPERS), WHOLE (SPICE) | 238UNSAFE ADD | San Francisco District Office (SAN-DO) |
| 2/24/2011 | 28AAH08CAPSICUMS (CAYENNE CHILI, HOT PEPPERS), WHOLE (SPICE) | 2920PESTICIDES | San Francisco District Office (SAN-DO) |
| 2/16/2011 | 28AAH08CAPSICUMS (CAYENNE CHILI, HOT PEPPERS), WHOLE (SPICE) | 2920PESTICIDES | San Francisco District Office (SAN-DO) |
| 1/20/2011 | 24HGH08PEPPER, HOT, DRIED OR PASTE | 2920PESTICIDES | Los Angeles District Office (LOS-DO) |
| 1/20/2011 | 24HGH08PEPPER, HOT, DRIED OR PASTE | 2920PESTICIDES | Los Angeles District Office (LOS-DO) |
| 12/9/2010 | 24HGH08PEPPER, HOT, DRIED OR PASTE | 2920PESTICIDES | Los Angeles District Office (LOS-DO) |
| 11/4/2010 | 24HGH08PEPPER, HOT, DRIED OR PASTE | 2920PESTICIDES | Los Angeles District Office (LOS-DO) |
| 10/20/2010 | 24HGH08PEPPER, HOT, DRIED OR PASTE | Los Angeles District Office (LOS-DO) |
Frequently Asked Questions
What is ITC LIMITED's FDA import refusal history?
ITC LIMITED (FEI: 3006292098) has 13 FDA import refusal record(s) in our database, spanning from 10/20/2010 to 3/23/2011.
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. ITC LIMITED's FEI number is 3006292098.
What types of violations has ITC LIMITED received?
ITC LIMITED has been cited for 3 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 ITC LIMITED come from?
All FDA import refusal data for ITC LIMITED 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.