Raj Foods International
FDA import alert and refusal historyUnjha, IndiaFEI 3007041566
As of October 26, 2026, Raj Foods International (Unjha, India) is on the red list of FDA Import Alert 99-08 (Processed human and animal foods: pesticides) for sesame seeds, published by FDA on November 7, 2012, and has 3 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
- Sesame seed (edible seed) · PESTICIDE
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Raj Foods International
4 records, newest first. Each line links to the FDA page it came from.
Refusal charges, in plain English
- PESTICIDE3 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 Raj Foods International
- Is Raj Foods International on an FDA import alert?
- Yes. As of October 26, 2026, Raj Foods International is on the red list of FDA Import Alert 99-08, “Processed human and animal foods: pesticides”, for sesame seeds; FDA published the listing on November 7, 2012.
- Has FDA refused shipments from Raj Foods International?
- Yes. FDA refused 3 shipment lines from Raj Foods International between May 15, 2017 and November 12, 2020. The most recent, on November 12, 2020, was sesame seed (edible seed), charged as PESTICIDE (pesticide chemical residue).
- Why did FDA refuse Raj Foods International's shipments?
- The most frequent charge is PESTICIDE (pesticide chemical residue, 3 lines).
- What is Raj Foods International's FEI number?
- Raj Foods International's FDA Establishment Identifier (FEI) is 3007041566.
- Can shipments from Raj Foods International still enter the U.S.?
- Shipments of sesame seeds from Raj Foods International 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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