CM Tech & Traders
FDA import alert and refusal historyCoimbatore, IndiaFEI 3013141717
As of October 26, 2026, CM Tech & Traders (Coimbatore, India) is on the red list of FDA Import Alert 99-19 (Food products: Salmonella) for green cardamom, published by FDA on April 24, 2017, and has 2 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
- Cardamon, whole (spice) · SALMONELLA
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for CM Tech & Traders
3 records, newest first. Each line links to the FDA page it came from.
2017
- Import refusalRefused, Cardamon, whole (spice)SALMONELLAEntry KM6-1503238-0Source
- Import alert listingListed on Import Alert 99-19red listGreen CardamomSource
- Import refusalRefused, Pepper,black, whole (spice)SALMONELLAEntry KM6-1503238-0Source
Refusal charges, in plain English
- SALMONELLA2 refused lines
Salmonella
The product appeared to contain Salmonella, which the law treats as a poisonous and deleterious substance that may make food injurious to health.
Questions about CM Tech & Traders
- Is CM Tech & Traders on an FDA import alert?
- Yes. As of October 26, 2026, CM Tech & Traders is on the red list of FDA Import Alert 99-19, “Food products: Salmonella”, for green cardamom; FDA published the listing on April 24, 2017.
- Has FDA refused shipments from CM Tech & Traders?
- Yes. FDA refused 2 shipment lines from CM Tech & Traders between April 4, 2017 and May 2, 2017. The most recent, on May 2, 2017, was cardamon, whole (spice), charged as SALMONELLA (salmonella).
- Why did FDA refuse CM Tech & Traders's shipments?
- The most frequent charge is SALMONELLA (salmonella, 2 lines).
- What is CM Tech & Traders's FEI number?
- CM Tech & Traders's FDA Establishment Identifier (FEI) is 3013141717.
- Can shipments from CM Tech & Traders still enter the U.S.?
- Shipments of green cardamom from CM Tech & Traders 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.