Salomi International
FDA import alert and refusal historyNavi Mumbai, IndiaFEI 3006427551
Recorded by FDA as SALOMI INTERNATIONAL
As of October 26, 2026, Salomi International (Navi Mumbai, India) is on the red list of FDA Import Alert 99-19 (Food products: Salmonella) for sesame seed (edible seed); cumin, whole (spice); sesame, whole (spice); cumin, ground, cracked (spice); sesame, ground, cracked (spice), published by FDA on September 16, 2009, 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 99-19 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Salomi International
1 record, newest first. Each line links to the FDA page it came from.
2009
- Import alert listingListed on Import Alert 99-19red listSesame Seed (Edible Seed); Cumin, Whole (Spice); Sesame, Whole (Spice); Cumin, Ground, Cracked (Spice); Sesame, Ground, Cracked (Spice)Source
Questions about Salomi International
- Is Salomi International on an FDA import alert?
- Yes. As of October 26, 2026, Salomi International is on the red list of FDA Import Alert 99-19, “Food products: Salmonella”, for sesame seed (edible seed); cumin, whole (spice); sesame, whole (spice); cumin, ground, cracked (spice); sesame, ground, cracked (spice); FDA published the listing on September 16, 2009.
- Has FDA refused shipments from Salomi International?
- No FDA import refusals for Salomi International appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Salomi International's FEI number?
- Salomi International's FDA Establishment Identifier (FEI) is 3006427551.
- Can shipments from Salomi International still enter the U.S.?
- Shipments of sesame seed (edible seed); cumin, whole (spice); sesame, whole (spice); cumin, ground, cracked (spice); sesame, ground, cracked (spice) from Salomi International 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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