Sams Fruit Products Pvt Ltd
FDA import alert and refusal historyMumbai, IndiaFEI 3006552522
As of October 26, 2026, Sams Fruit Products Pvt Ltd (Mumbai, India) is on the red list of FDA Import Alert 45-02 (Foods with illegal or undeclared colors) for mint chutney; chutney; green bhel chutney; condiments, n.e.c.; coriander, ground, cracked (spice), published by FDA on September 18, 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 45-02 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Sams Fruit Products Pvt Ltd
1 record, newest first. Each line links to the FDA page it came from.
2009
- Import alert listingListed on Import Alert 45-02red listmint chutney; Chutney; green bhel chutney; Condiments, N.E.C.; Coriander, Ground, Cracked (Spice)Source
Questions about Sams Fruit Products Pvt Ltd
- Is Sams Fruit Products Pvt Ltd on an FDA import alert?
- Yes. As of October 26, 2026, Sams Fruit Products Pvt Ltd is on the red list of FDA Import Alert 45-02, “Foods with illegal or undeclared colors”, for mint chutney; chutney; green bhel chutney; condiments, n.e.c.; coriander, ground, cracked (spice); FDA published the listing on September 18, 2009.
- Has FDA refused shipments from Sams Fruit Products Pvt Ltd?
- No FDA import refusals for Sams Fruit Products Pvt Ltd appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Sams Fruit Products Pvt Ltd's FEI number?
- Sams Fruit Products Pvt Ltd's FDA Establishment Identifier (FEI) is 3006552522.
- Can shipments from Sams Fruit Products Pvt Ltd still enter the U.S.?
- Shipments of mint chutney; chutney; green bhel chutney; condiments, n.e.c.; coriander, ground, cracked (spice) from Sams Fruit Products Pvt Ltd can be detained without physical examination under Import Alert 45-02; 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.