Muntimadugu Rama Mani
FDA import alert and refusal historyAnantapur Urban, IndiaFEI 3040301562
Recorded by FDA as MUNTIMADUGU RAMA MANI
As of October 26, 2026, Muntimadugu Rama Mani is not on any FDA import alert in SupplierRadar's records; FDA refused 2 of its shipment lines on November 10, 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
- Tamarind (subtropical and tropical fruit) · FILTHY
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Muntimadugu Rama Mani
2 records, newest first. Each line links to the FDA page it came from.
2025
- Import refusalSource
Refused, 2 lines in one entry: Tamarind (subtropical and tropical fruit); Other bakery products, n.e.c.FILTHYEntry SCS-5947664-3Show 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 Muntimadugu Rama Mani
- Is Muntimadugu Rama Mani on an FDA import alert?
- No listing for Muntimadugu Rama Mani 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 Muntimadugu Rama Mani?
- Yes. FDA refused 2 shipment lines from Muntimadugu Rama Mani on November 10, 2025. The most recent, on November 10, 2025, was tamarind (subtropical and tropical fruit), charged as FILTHY (filthy, putrid or decomposed substance).
- Why did FDA refuse Muntimadugu Rama Mani's shipments?
- The most frequent charge is FILTHY (filthy, putrid or decomposed substance, 2 lines).
- What is Muntimadugu Rama Mani's FEI number?
- Muntimadugu Rama Mani's FDA Establishment Identifier (FEI) is 3040301562.
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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.