Kp Overseas
FDA import alert and refusal historyMumbai, IndiaFEI 3004630914
As of October 25, 2026, Kp Overseas (Mumbai, India) is on the red list of FDA Import Alert 99-19 (Food products: Salmonella) for chili powder hot; ground coriander; turmeric powder, published by FDA on March 22, 2013, is also listed on Import Alert 45-02 (red list), 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 listIA 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 Kp Overseas
2 records, newest first. Each line links to the FDA page it came from.
2013
- Import alert listingListed on Import Alert 99-19red listChili Powder Hot; Ground Coriander; Turmeric PowderSource
2012
- Import alert listingListed on Import Alert 45-02red listMukhwas Green Mixed edible seeds Breath Freshener; Mukhwas Red Mixed edible seeds Breath FreshenerSource
Questions about Kp Overseas
- Is Kp Overseas on an FDA import alert?
- Yes. As of October 25, 2026, Kp Overseas is on the red list of FDA Import Alert 99-19, “Food products: Salmonella”, for chili powder hot; ground coriander; turmeric powder; FDA published the listing on March 22, 2013.
- Has FDA refused shipments from Kp Overseas?
- No FDA import refusals for Kp Overseas appear in FDA's refusal data since October 2016, as of October 25, 2026.
- What is Kp Overseas's FEI number?
- Kp Overseas's FDA Establishment Identifier (FEI) is 3004630914.
- Can shipments from Kp Overseas still enter the U.S.?
- Shipments of chili powder hot; ground coriander; turmeric powder from Kp Overseas 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.