Has FDA refused shipments from JKM Enterprise Private Limited?

Yes. FDA refused 5 shipment lines from JKM Enterprise Private Limited between January 25, 2019 and February 27, 2026. The most recent, on February 27, 2026, was tamarind, dried or paste, charged as FILTHY (filthy, putrid or decomposed substance).

Why did FDA refuse JKM Enterprise Private Limited's shipments?

The most frequent charges are SALMONELLA (salmonella, 3 lines) and FILTHY (filthy, putrid or decomposed substance, 2 lines).

What is JKM Enterprise Private Limited's FEI number?

JKM Enterprise Private Limited's FDA Establishment Identifier (FEI) is 3011525332.

Can shipments from JKM Enterprise Private Limited still enter the U.S.?

Shipments of spl mixture from JKM Enterprise Private Limited 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).

JKM Enterprise Private Limited

FDA import alert and refusal historyChennai, IndiaFEI 3011525332

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As of October 26, 2026, JKM Enterprise Private Limited (Chennai, India) is on the red list of FDA Import Alert 99-19 (Food products: Salmonella) for spl mixture, published by FDA on May 12, 2017, and has 5 FDA import refusals recorded since October 2016.

Data from FDA public records, last checked October 26, 2026. Request a correction

Current status

Import alerts: IA 99-19 · red list
Last import refusal: Feb 27, 2026Tamarind, dried or paste · FILTHY
Last warning letter: None found
Last inspection: None on record

Every FDA record for JKM Enterprise Private Limited

6 records, newest first. Each line links to the FDA page it came from.

2026

Feb 27, 2026Import refusal
Refused, 2 lines in one entry: Tamarind, dried or pasteFILTHYEntry H77-0238342-0Show 2 linesHide lines
- Refused, Tamarind, dried or pasteFILTHYEntry H77-0238342-0Source
- Refused, Tamarind, dried or pasteFILTHYEntry H77-0238342-0Source
Source

2022

Feb 7, 2022Import refusal
Refused, Candy specialties, n.e.c. (without chocolate)SALMONELLAEntry 8KP-0019903-5
Source

2019

Oct 3, 2019Import refusal
Refused, Pepper,black, whole (spice)SALMONELLAEntry B9G-0011400-1
Source
Jan 25, 2019Import refusal
Refused, Tropical mixed vegetables, with sauceSALMONELLAEntry WD8-0061906-2
Source

2017

May 12, 2017Import alert listing
Listed on Import Alert 99-19red listSPL Mixture
Source

Refusal charges, in plain English

SALMONELLA3 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.
FILTHY2 refused lines
Filthy, putrid or decomposed substance
The product appeared to consist in whole or in part of a filthy, putrid, or decomposed substance, or to be otherwise unfit for food.

Questions about JKM Enterprise Private Limited

Is JKM Enterprise Private Limited on an FDA import alert?: Yes. As of October 26, 2026, JKM Enterprise Private Limited is on the red list of FDA Import Alert 99-19, “Food products: Salmonella”, for spl mixture; FDA published the listing on May 12, 2017.
Has FDA refused shipments from JKM Enterprise Private Limited?: Yes. FDA refused 5 shipment lines from JKM Enterprise Private Limited between January 25, 2019 and February 27, 2026. The most recent, on February 27, 2026, was tamarind, dried or paste, charged as FILTHY (filthy, putrid or decomposed substance).
Why did FDA refuse JKM Enterprise Private Limited's shipments?: The most frequent charges are SALMONELLA (salmonella, 3 lines) and FILTHY (filthy, putrid or decomposed substance, 2 lines).
What is JKM Enterprise Private Limited's FEI number?: JKM Enterprise Private Limited's FDA Establishment Identifier (FEI) is 3011525332.
Can shipments from JKM Enterprise Private Limited still enter the U.S.?: Shipments of spl mixture from JKM Enterprise Private Limited 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.