Om Satya overseas
FDA import alert and refusal historyKachwa,Tehsil, IndiaFEI 3013002752
As of October 26, 2026, Om Satya overseas (KACHWA,TEHSIL, 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 May 26, 2020, and has 4 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 Om Satya overseas
5 records, newest first. Each line links to the FDA page it came from.
2020
2019
Refusal charges, in plain English
- PESTICIDE4 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 Om Satya overseas
- Is Om Satya overseas on an FDA import alert?
- Yes. As of October 26, 2026, Om Satya overseas 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 May 26, 2020.
- Has FDA refused shipments from Om Satya overseas?
- Yes. FDA refused 4 shipment lines from Om Satya overseas between July 18, 2019 and March 27, 2020. The most recent, on March 27, 2020, was rice, basmati, processed (packaged), charged as PESTICIDE (pesticide chemical residue).
- Why did FDA refuse Om Satya overseas's shipments?
- The most frequent charge is PESTICIDE (pesticide chemical residue, 4 lines).
- What is Om Satya overseas's FEI number?
- Om Satya overseas's FDA Establishment Identifier (FEI) is 3013002752.
- Can shipments from Om Satya overseas still enter the U.S.?
- Shipments of basmati rice from Om Satya overseas 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.