Mondelez India Foods Limited
FDA import alert and refusal historySolan, IndiaFEI 3013957610
Recorded by FDA as MONDELEZ INDIA FOODS LIMITED
As of October 27, 2026, Mondelez India Foods Limited is not on any FDA import alert in SupplierRadar's records; FDA refused 2 of its shipment lines on April 6, 2018, most often for filthy, putrid or decomposed substance (FILTHY).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- Chocolate and cocoa beverage base, n.e.c. · FILTHY
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Mondelez India Foods Limited
2 records, newest first. Each line links to the FDA page it came from.
2018
- Import refusalSource
Refused, 2 lines in one entry: Chocolate and cocoa beverage base, n.e.c.FILTHYEntry EVJ-0213781-1Show 2 linesHide lines
Refusal charges, in plain English
- 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 Mondelez India Foods Limited
- Is Mondelez India Foods Limited on an FDA import alert?
- No listing for Mondelez India Foods Limited appears in the FDA import alerts SupplierRadar checked on October 27, 2026. Country-wide alerts may still apply to its products; see the India page.
- Has FDA refused shipments from Mondelez India Foods Limited?
- Yes. FDA refused 2 shipment lines from Mondelez India Foods Limited on April 6, 2018. The most recent, on April 6, 2018, was chocolate and cocoa beverage base, n.e.c., charged as FILTHY (filthy, putrid or decomposed substance).
- Why did FDA refuse Mondelez India Foods Limited's shipments?
- The most frequent charge is FILTHY (filthy, putrid or decomposed substance, 2 lines).
- What is Mondelez India Foods Limited's FEI number?
- Mondelez India Foods Limited's FDA Establishment Identifier (FEI) is 3013957610.
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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.