DCP India
FDA import alert and refusal historyRevenue Estate, IndiaFEI 3010962228
As of October 26, 2026, DCP India (Revenue Estate, India) is on the red list of FDA Import Alert 99-08 (Processed human and animal foods: pesticides) for basmati rice, published by FDA on March 9, 2018, and has 2 FDA import refusals recorded since October 2016.
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- IA 99-08 · red list
- Last import refusal
- Rice, basmati, processed (packaged) · PESTICIDE
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for DCP India
3 records, newest first. Each line links to the FDA page it came from.
Refusal charges, in plain English
- PESTICIDE2 refused lines
Pesticide chemical residue
The product appeared to contain a pesticide chemical residue that makes it adulterated under section 402(a)(2)(B) of the FD&C Act, for example a residue above the U.S. tolerance or one with no U.S. tolerance for that food.
Questions about DCP India
- Is DCP India on an FDA import alert?
- Yes. As of October 26, 2026, DCP India is on the red list of FDA Import Alert 99-08, “Processed human and animal foods: pesticides”, for basmati rice; FDA published the listing on March 9, 2018.
- Has FDA refused shipments from DCP India?
- Yes. FDA refused 2 shipment lines from DCP India between February 26, 2018 and June 25, 2018. The most recent, on June 25, 2018, was rice, basmati, processed (packaged), charged as PESTICIDE (pesticide chemical residue).
- Why did FDA refuse DCP India's shipments?
- The most frequent charge is PESTICIDE (pesticide chemical residue, 2 lines).
- What is DCP India's FEI number?
- DCP India's FDA Establishment Identifier (FEI) is 3010962228.
- Can shipments from DCP India still enter the U.S.?
- Shipments of basmati rice from DCP India can be detained without physical examination under Import Alert 99-08; FDA releases them only if evidence shows they do not have the listed violation. Importers must consider this listing in their FSVP evaluation (21 CFR 1.505).
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SupplierRadar is not affiliated with the U.S. Food and Drug Administration. Data comes from public FDA records and may contain errors. This is not legal advice; importers remain responsible for their supplier evaluations.