Jalaram Gruh Udyog
FDA import alert and refusal historyMumbai, IndiaFEI 3017883403
As of October 26, 2026, Jalaram Gruh Udyog (Mumbai, India) is on the red list of FDA Import Alert 99-19 (Food products: Salmonella) for mumbai missal, instant 2 minutes missal mix, published by FDA on July 27, 2026, 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
- Bread snacks, n.e.c. · SALMONELLA
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Jalaram Gruh Udyog
2 records, newest first. Each line links to the FDA page it came from.
2026
- Import alert listingListed on Import Alert 99-19red listMumbai Missal, Instant 2 Minutes Missal MixSource
- Import refusalRefused, Bread snacks, n.e.c.SALMONELLAEntry 8RG-2688159-5Source
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 Jalaram Gruh Udyog
- Is Jalaram Gruh Udyog on an FDA import alert?
- Yes. As of October 26, 2026, Jalaram Gruh Udyog is on the red list of FDA Import Alert 99-19, “Food products: Salmonella”, for mumbai missal, instant 2 minutes missal mix; FDA published the listing on July 27, 2026.
- Has FDA refused shipments from Jalaram Gruh Udyog?
- Yes. FDA refused 1 shipment line from Jalaram Gruh Udyog on July 27, 2026. The most recent, on July 27, 2026, was bread snacks, n.e.c., charged as SALMONELLA (salmonella).
- Why did FDA refuse Jalaram Gruh Udyog's shipments?
- The most frequent charge is SALMONELLA (salmonella, 1 line).
- What is Jalaram Gruh Udyog's FEI number?
- Jalaram Gruh Udyog's FDA Establishment Identifier (FEI) is 3017883403.
- Can shipments from Jalaram Gruh Udyog still enter the U.S.?
- Shipments of mumbai missal, instant 2 minutes missal mix from Jalaram Gruh Udyog 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.