Godrej Industries Limited - Foods Division
FDA import alert and refusal historyMandideep.Distt.Raisen, IndiaFEI 3004692120
Recorded by FDA as GODREJ INDUSTRIES LIMITED - FOODS DIVISION
As of October 26, 2026, Godrej Industries Limited - Foods Division (Mandideep.Distt.Raisen, India) is on the red list of FDA Import Alert 45-02 (Foods with illegal or undeclared colors) for custard; custard powder vanilla; custard pudding mix, published by FDA on September 18, 2009, and has no 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
- None since October 2016
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Godrej Industries Limited - Foods Division
1 record, newest first. Each line links to the FDA page it came from.
2009
- Import alert listingListed on Import Alert 45-02red listCustard; Custard Powder Vanilla; Custard Pudding MixSource
Questions about Godrej Industries Limited - Foods Division
- Is Godrej Industries Limited - Foods Division on an FDA import alert?
- Yes. As of October 26, 2026, Godrej Industries Limited - Foods Division is on the red list of FDA Import Alert 45-02, “Foods with illegal or undeclared colors”, for custard; custard powder vanilla; custard pudding mix; FDA published the listing on September 18, 2009.
- Has FDA refused shipments from Godrej Industries Limited - Foods Division?
- No FDA import refusals for Godrej Industries Limited - Foods Division appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Godrej Industries Limited - Foods Division's FEI number?
- Godrej Industries Limited - Foods Division's FDA Establishment Identifier (FEI) is 3004692120.
- Can shipments from Godrej Industries Limited - Foods Division still enter the U.S.?
- Shipments of custard; custard powder vanilla; custard pudding mix from Godrej Industries Limited - Foods Division 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.