M.R. Agro Industries
FDA import alert and refusal historyUnjha, IndiaFEI 3012138583
As of October 25, 2026, M.R. Agro Industries (Unjha, India) is on the red list of FDA Import Alert 99-19 (Food products: Salmonella) for sesame seed, published by FDA on July 2, 2021, and has 1 FDA import refusal recorded since October 2016.
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- IA 99-19 · red list
- Last import refusal
- Sesame seed (edible seed) · SALMONELLA
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for M.R. Agro Industries
2 records, newest first. Each line links to the FDA page it came from.
2021
- Import refusalRefused, Sesame seed (edible seed)SALMONELLAEntry 164-0287865-2Source
- Import alert listingListed on Import Alert 99-19red listSesame SeedSource
Refusal charges, in plain English
- SALMONELLA1 refused line
Salmonella
The product appeared to contain Salmonella, which the law treats as a poisonous and deleterious substance that may make food injurious to health.
Questions about M.R. Agro Industries
- Is M.R. Agro Industries on an FDA import alert?
- Yes. As of October 25, 2026, M.R. Agro Industries is on the red list of FDA Import Alert 99-19, “Food products: Salmonella”, for sesame seed; FDA published the listing on July 2, 2021.
- Has FDA refused shipments from M.R. Agro Industries?
- Yes. FDA refused 1 shipment line from M.R. Agro Industries on November 5, 2021. The most recent, on November 5, 2021, was sesame seed (edible seed), charged as SALMONELLA (salmonella).
- Why did FDA refuse M.R. Agro Industries's shipments?
- The most frequent charge is SALMONELLA (salmonella, 1 line).
- What is M.R. Agro Industries's FEI number?
- M.R. Agro Industries's FDA Establishment Identifier (FEI) is 3012138583.
- Can shipments from M.R. Agro Industries still enter the U.S.?
- Shipments of sesame seed from M.R. Agro Industries can be detained without physical examination under Import Alert 99-19; 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.