Vks Hytech Private Limited
FDA import alert and refusal historyPanchkula, IndiaFEI 3038628034
Recorded by FDA as VKS HYTECH PRIVATE LIMITED
As of October 26, 2026, Vks Hytech Private Limited (Panchkula, India) is on the red list of FDA Import Alert 45-02 (Foods with illegal or undeclared colors) for kaju casatta; imarti; mango barfi; motichoor laddu; special pista roll, published by FDA on September 30, 2025, and has 5 FDA import refusals recorded since October 2016.
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- IA 45-02 · red list
- Last import refusal
- Other bakery products, n.e.c. · UNSAFE COL
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Vks Hytech Private Limited
6 records, newest first. Each line links to the FDA page it came from.
2025
- Import refusalSource
Refused, 5 lines in one entry: Other bakery products, n.e.c.; Fried snack foods, n.e.c. and 1 moreUNSAFE COLLIST INGRELACKS N/CNUTRIT LBLEntry MK8-6029160-0Show 5 linesHide lines
- Refused, Other bakery products, n.e.c.UNSAFE COLLIST INGRELACKS N/CNUTRIT LBLEntry MK8-6029160-0Source
- Refused, Fried snack foods, n.e.c.UNSAFE COLLIST INGRELACKS N/CNUTRIT LBLYELLOW #5Entry MK8-6029160-0Source
- Refused, Sweet goods without custard or cream filling, n.e.c.UNSAFE COLLIST INGRELACKS N/CNUTRIT LBLYELLOW #5Entry MK8-6029160-0Source
- Refused, Sweet goods without custard or cream filling, n.e.c.UNSAFE COLLIST INGRELACKS N/CNUTRIT LBLYELLOW #5Entry MK8-6029160-0Source
- Refused, Fried snack foods, n.e.c.UNSAFE COLLIST INGRELACKS N/CNUTRIT LBLYELLOW #5Entry MK8-6029160-0Source
- Import alert listingListed on Import Alert 45-02red listKaju casatta; imarti; mango barfi; motichoor laddu; special pista rollSource
Refusal charges, in plain English
- LACKS N/C5 refused lines
Net quantity statement missing
The packaged food appeared not to carry an accurate statement of the quantity of contents, such as net weight, measure, or count, on its label.
- LIST INGRE5 refused lines
Ingredients not listed
The product is made from two or more ingredients and the label appeared not to list the common or usual name of each one (or, for a juice beverage, the percentage of juice).
- NUTRIT LBL5 refused lines
Nutrition information missing from label
The label or labeling appeared not to carry the nutrition information that U.S. law requires for the food.
- UNSAFE COL5 refused lines
Color additive unsafe under section 721
The product appeared to be, or to contain, a color additive that is unsafe within the meaning of section 721(a) of the FD&C Act, the section that governs which color additives may be used and how.
- YELLOW #54 refused lines
FD&C Yellow No. 5 not declared
The food appeared to contain the color additive FD&C Yellow No. 5 without declaring it on the label as 21 CFR 74.705 requires.
Questions about Vks Hytech Private Limited
- Is Vks Hytech Private Limited on an FDA import alert?
- Yes. As of October 26, 2026, Vks Hytech Private Limited is on the red list of FDA Import Alert 45-02, “Foods with illegal or undeclared colors”, for kaju casatta; imarti; mango barfi; motichoor laddu; special pista roll; FDA published the listing on September 30, 2025.
- Has FDA refused shipments from Vks Hytech Private Limited?
- Yes. FDA refused 5 shipment lines from Vks Hytech Private Limited on October 9, 2025. The most recent, on October 9, 2025, was other bakery products, n.e.c., charged as UNSAFE COL (color additive unsafe under section 721).
- Why did FDA refuse Vks Hytech Private Limited's shipments?
- The most frequent charges are LACKS N/C (net quantity statement missing, 5 lines) and LIST INGRE (ingredients not listed, 5 lines).
- What is Vks Hytech Private Limited's FEI number?
- Vks Hytech Private Limited's FDA Establishment Identifier (FEI) is 3038628034.
- Can shipments from Vks Hytech Private Limited still enter the U.S.?
- Shipments of kaju casatta; imarti; mango barfi; motichoor laddu; special pista roll from Vks Hytech Private Limited can be detained without physical examination under Import Alert 45-02; 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.