Suminter India Organics Pvt Ltd
FDA import alert and refusal historyAdimali Po Idukki District, IndiaFEI 3004299656
As of October 26, 2026, Suminter India Organics Pvt Ltd (Adimali Po Idukki District, India) is on the red list of FDA Import Alert 99-05 (Raw agricultural products: pesticides) for soybeans, whole grain, published by FDA on September 16, 2009, is also listed on Import Alert 99-19 (red list), and has no FDA import refusals recorded since October 2016.
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- IA 99-05 · red listIA 99-19 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Suminter India Organics Pvt Ltd
2 records, newest first. Each line links to the FDA page it came from.
2009
- Import alert listingListed on Import Alert 99-19red listcrushed red chiliSource
- Import alert listingListed on Import Alert 99-05red listSoybeans, Whole GrainSource
Questions about Suminter India Organics Pvt Ltd
- Is Suminter India Organics Pvt Ltd on an FDA import alert?
- Yes. As of October 26, 2026, Suminter India Organics Pvt Ltd is on the red list of FDA Import Alert 99-05, “Raw agricultural products: pesticides”, for soybeans, whole grain; FDA published the listing on September 16, 2009.
- Has FDA refused shipments from Suminter India Organics Pvt Ltd?
- No FDA import refusals for Suminter India Organics Pvt Ltd appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Suminter India Organics Pvt Ltd's FEI number?
- Suminter India Organics Pvt Ltd's FDA Establishment Identifier (FEI) is 3004299656.
- Can shipments from Suminter India Organics Pvt Ltd still enter the U.S.?
- Shipments of soybeans, whole grain from Suminter India Organics Pvt Ltd can be detained without physical examination under Import Alert 99-05; 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.