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Shri Ganesh Gruh

FDA import alert and refusal historyUttarbanda, IndiaFEI 3020897663

Recorded by FDA as SHRI GANESH GRUH

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Example subjectShri Ganesh Gru added to Import Alert 16-129 (red list)

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As of October 26, 2026, Shri Ganesh Gruh is not on any FDA import alert in SupplierRadar's records; FDA refused 7 of its shipment lines on September 5, 2025, 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
Crackers (non filled) n.e.c. · FILTHY
Last warning letter
None found
Last inspection
None on record

Every FDA record for Shri Ganesh Gruh

7 records, newest first. Each line links to the FDA page it came from.

2025

  1. Import refusal
    Refused, 7 lines in one entry: Crackers (non filled) n.e.c.; PapadFILTHYEntry KM6-3657294-3Show 7 lines
    Source

Refusal charges, in plain English

  • FILTHY7 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 Shri Ganesh Gruh

Is Shri Ganesh Gruh on an FDA import alert?
No listing for Shri Ganesh Gruh 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 Shri Ganesh Gruh?
Yes. FDA refused 7 shipment lines from Shri Ganesh Gruh on September 5, 2025. The most recent, on September 5, 2025, was crackers (non filled) n.e.c., charged as FILTHY (filthy, putrid or decomposed substance).
Why did FDA refuse Shri Ganesh Gruh's shipments?
The most frequent charge is FILTHY (filthy, putrid or decomposed substance, 7 lines).
What is Shri Ganesh Gruh's FEI number?
Shri Ganesh Gruh's FDA Establishment Identifier (FEI) is 3020897663.

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Example subjectShri Ganesh Gru added to Import Alert 16-129 (red list)

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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.