Tata Tea Limited, Instant Tea Division
FDA import alert and refusal historyKochi, IndiaFEI 1000394360
As of October 26, 2026, Tata Tea Limited, Instant Tea Division (Kochi, India) is on the red list of FDA Import Alert 99-19 (Food products: Salmonella) for nutmeg, 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 Tata Tea Limited, Instant Tea Division
1 record, newest first. Each line links to the FDA page it came from.
2009
- Import alert listingListed on Import Alert 99-19red listNutmeg, Ground, Cracked (Spice)Source
Questions about Tata Tea Limited, Instant Tea Division
- Is Tata Tea Limited, Instant Tea Division on an FDA import alert?
- Yes. As of October 26, 2026, Tata Tea Limited, Instant Tea Division is on the red list of FDA Import Alert 99-19, “Food products: Salmonella”, for nutmeg, ground, cracked (spice); FDA published the listing on September 16, 2009.
- Has FDA refused shipments from Tata Tea Limited, Instant Tea Division?
- No FDA import refusals for Tata Tea Limited, Instant Tea Division appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Tata Tea Limited, Instant Tea Division's FEI number?
- Tata Tea Limited, Instant Tea Division's FDA Establishment Identifier (FEI) is 1000394360.
- Can shipments from Tata Tea Limited, Instant Tea Division still enter the U.S.?
- Shipments of nutmeg, ground, cracked (spice) from Tata Tea Limited, Instant Tea Division 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.