SinghInt
FDA import alert and refusal historyMumbai, IndiaFEI 3013395611
As of October 26, 2026, SinghInt (Mumbai, India) is on the red list of FDA Import Alert 99-19 (Food products: Salmonella) for kali jeeri (black cumin), published by FDA on September 14, 2017, 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
- Black cumin, natural extract or flavor (spice) · SALMONELLA
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for SinghInt
2 records, newest first. Each line links to the FDA page it came from.
2017
- Import alert listingListed on Import Alert 99-19red listKali Jeeri (black cumin)Source
- Import refusalRefused, Black cumin, natural extract or flavor (spice)SALMONELLAEntry 224-3092841-0Source
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 SinghInt
- Is SinghInt on an FDA import alert?
- Yes. As of October 26, 2026, SinghInt is on the red list of FDA Import Alert 99-19, “Food products: Salmonella”, for kali jeeri (black cumin); FDA published the listing on September 14, 2017.
- Has FDA refused shipments from SinghInt?
- Yes. FDA refused 1 shipment line from SinghInt on September 14, 2017. The most recent, on September 14, 2017, was black cumin, natural extract or flavor (spice), charged as SALMONELLA (salmonella).
- Why did FDA refuse SinghInt's shipments?
- The most frequent charge is SALMONELLA (salmonella, 1 line).
- What is SinghInt's FEI number?
- SinghInt's FDA Establishment Identifier (FEI) is 3013395611.
- Can shipments from SinghInt still enter the U.S.?
- Shipments of kali jeeri (black cumin) from SinghInt 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.