Devi Exports Pvt Ltd
FDA import alert and refusal historyAmritsar, IndiaFEI 3005428233
As of October 26, 2026, Devi Exports Pvt Ltd (Amritsar, India) is on the red list of FDA Import Alert 99-19 (Food products: Salmonella) for turmeric powder (haldi powder), published by FDA on January 21, 2011, 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 Devi Exports Pvt Ltd
2 records, newest first. Each line links to the FDA page it came from.
2011
- Import alert listingListed on Import Alert 99-19red listTurmeric Powder (Haldi Powder)Source
2009
- Import alert listingListed on Import Alert 45-02red listFennel, Whole (Spice); Hard Candy without Nuts and Fruit, N.E.C. (without Chocolate)Source
Questions about Devi Exports Pvt Ltd
- Is Devi Exports Pvt Ltd on an FDA import alert?
- Yes. As of October 26, 2026, Devi Exports Pvt Ltd is on the red list of FDA Import Alert 99-19, “Food products: Salmonella”, for turmeric powder (haldi powder); FDA published the listing on January 21, 2011.
- Has FDA refused shipments from Devi Exports Pvt Ltd?
- No FDA import refusals for Devi Exports Pvt Ltd appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Devi Exports Pvt Ltd's FEI number?
- Devi Exports Pvt Ltd's FDA Establishment Identifier (FEI) is 3005428233.
- Can shipments from Devi Exports Pvt Ltd still enter the U.S.?
- Shipments of turmeric powder (haldi powder) from Devi Exports Pvt Ltd 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.