Adhik Rangoli Foods Exim Private Limited
FDA import alert and refusal historyChakan, IndiaFEI 3018011397
As of October 26, 2026, Adhik Rangoli Foods Exim Private Limited is not on any FDA import alert in SupplierRadar's records; FDA refused 2 of its shipment lines between February 1, 2021 and January 10, 2023, 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
- Pepper, black, ground, cracked (spice) · FILTHY
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Adhik Rangoli Foods Exim Private Limited
2 records, newest first. Each line links to the FDA page it came from.
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 Adhik Rangoli Foods Exim Private Limited
- Is Adhik Rangoli Foods Exim Private Limited on an FDA import alert?
- No listing for Adhik Rangoli Foods Exim Private Limited appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the India page.
- Has FDA refused shipments from Adhik Rangoli Foods Exim Private Limited?
- Yes. FDA refused 2 shipment lines from Adhik Rangoli Foods Exim Private Limited between February 1, 2021 and January 10, 2023. The most recent, on January 10, 2023, was pepper, black, ground, cracked (spice), charged as FILTHY (filthy, putrid or decomposed substance).
- Why did FDA refuse Adhik Rangoli Foods Exim Private Limited's shipments?
- The most frequent charge is FILTHY (filthy, putrid or decomposed substance, 2 lines).
- What is Adhik Rangoli Foods Exim Private Limited's FEI number?
- Adhik Rangoli Foods Exim Private Limited's FDA Establishment Identifier (FEI) is 3018011397.
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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.