K & B Manufacturing
FDA import alert and refusal historyAhmedabad, IndiaFEI 3010242733
As of October 26, 2026, K & B Manufacturing (Ahmedabad, India) is on the red list of FDA Import Alert 99-39 (Imported foods that appear to be misbranded) for vegetable cooking oil, published by FDA on September 1, 2022, is also listed on Import Alert 99-22 (red list), and has 3 FDA import refusals recorded since October 2016.
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- IA 99-39 · red listIA 99-22 · red list
- Last import refusal
- Snack foods not elsewhere mentioned, n.e.c. · COLOR LBLG
- Last warning letter
- None found
- Last inspection
- Classified NAI (No Action Indicated)
Every FDA record for K & B Manufacturing
6 records, newest first. Each line links to the FDA page it came from.
2022
- Import alert listingListed on Import Alert 99-39red listVegetable cooking oilSource
- Import alert listingListed on Import Alert 99-22red listVegetable cooking oilSource
2019
- Import refusalRefused, Snack foods not elsewhere mentioned, n.e.c.COLOR LBLGEntry KM6-3526792-5Source
- Import refusalRefused, Snack foods not elsewhere mentioned, n.e.c.FILTHYEntry KM6-3523980-9Source
2018
- InspectionInspection classified NAI (No Action Indicated)Foodborne Biological HazardsSource
2017
- Import refusalRefused, Sauces, n.e.c.NEEDS FCENO PROCESSEntry KM6-3505234-3Source
Refusal charges, in plain English
- COLOR LBLG1 refused line
Artificial coloring not declared
The product appeared to contain an artificial coloring without labeling that states that fact.
- FILTHY1 refused line
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.
- NEEDS FCE1 refused line
Processor not registered for canned or acidified foods
The manufacturer appeared not to be registered with FDA as a low-acid canned food or acidified food processor, as 21 CFR 108.25 and 108.35 require.
- NO PROCESS1 refused line
No scheduled process filed
The manufacturer appeared not to have filed a scheduled process with FDA, which 21 CFR Part 108 requires for low-acid canned and acidified foods, so the product is treated as made under insanitary conditions.
Questions about K & B Manufacturing
- Is K & B Manufacturing on an FDA import alert?
- Yes. As of October 26, 2026, K & B Manufacturing is on the red list of FDA Import Alert 99-39, “Imported foods that appear to be misbranded”, for vegetable cooking oil; FDA published the listing on September 1, 2022.
- Has FDA refused shipments from K & B Manufacturing?
- Yes. FDA refused 3 shipment lines from K & B Manufacturing between July 28, 2017 and July 10, 2019. The most recent, on July 10, 2019, was snack foods not elsewhere mentioned, n.e.c., charged as COLOR LBLG (artificial coloring not declared).
- Why did FDA refuse K & B Manufacturing's shipments?
- The most frequent charges are COLOR LBLG (artificial coloring not declared, 1 line) and FILTHY (filthy, putrid or decomposed substance, 1 line).
- When was K & B Manufacturing last inspected by FDA?
- FDA's most recent inspection of K & B Manufacturing with a final classification is dated August 24, 2018 and was classified NAI (No Action Indicated).
- What is K & B Manufacturing's FEI number?
- K & B Manufacturing's FDA Establishment Identifier (FEI) is 3010242733.
- Can shipments from K & B Manufacturing still enter the U.S.?
- Shipments of vegetable cooking oil from K & B Manufacturing can be detained without physical examination under Import Alert 99-39; 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.