G.N. Products
FDA import alert and refusal historyUlhasnagar, IndiaFEI 3004320801
As of October 26, 2026, G.N. Products (Ulhasnagar, India) is on the red list of FDA Import Alert 45-02 (Foods with illegal or undeclared colors) for sago frittuers, published by FDA on July 1, 2016, and has 1 FDA import refusal 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. · FILTHY
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for G.N. Products
2 records, newest first. Each line links to the FDA page it came from.
2018
2016
- Import alert listingListed on Import Alert 45-02red listSago FrittuersSource
Refusal charges, in plain English
- 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.
Questions about G.N. Products
- Is G.N. Products on an FDA import alert?
- Yes. As of October 26, 2026, G.N. Products is on the red list of FDA Import Alert 45-02, “Foods with illegal or undeclared colors”, for sago frittuers; FDA published the listing on July 1, 2016.
- Has FDA refused shipments from G.N. Products?
- Yes. FDA refused 1 shipment line from G.N. Products on October 15, 2018. The most recent, on October 15, 2018, was other bakery products, n.e.c., charged as FILTHY (filthy, putrid or decomposed substance).
- Why did FDA refuse G.N. Products's shipments?
- The most frequent charge is FILTHY (filthy, putrid or decomposed substance, 1 line).
- What is G.N. Products's FEI number?
- G.N. Products's FDA Establishment Identifier (FEI) is 3004320801.
- Can shipments from G.N. Products still enter the U.S.?
- Shipments of sago frittuers from G.N. Products 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.