SupplierRadar

M V S L Pavan Kumar

FDA import alert and refusal historyVijayawada (Urban), IndiaFEI 3048201748

Recorded by FDA as M V S L PAVAN KUMAR

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Example subjectM V S L Pavan Kuma added to Import Alert 16-129 (red list)

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As of October 26, 2026, M V S L Pavan Kumar is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on September 17, 2026, 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, dried or paste · FILTHY
Last warning letter
None found
Last inspection
None on record

Every FDA record for M V S L Pavan Kumar

1 record, newest first. Each line links to the FDA page it came from.

2026

  1. Import refusal
    Refused, Tamarind, dried or pasteFILTHYEntry SCS-7522631-4
    Source

Refusal charges, in plain English

  • FILTHY1 refused line

    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 M V S L Pavan Kumar

Is M V S L Pavan Kumar on an FDA import alert?
No listing for M V S L Pavan Kumar 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 M V S L Pavan Kumar?
Yes. FDA refused 1 shipment line from M V S L Pavan Kumar on September 17, 2026. The most recent, on September 17, 2026, was tamarind, dried or paste, charged as FILTHY (filthy, putrid or decomposed substance).
Why did FDA refuse M V S L Pavan Kumar's shipments?
The most frequent charge is FILTHY (filthy, putrid or decomposed substance, 1 line).
What is M V S L Pavan Kumar's FEI number?
M V S L Pavan Kumar's FDA Establishment Identifier (FEI) is 3048201748.

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Example subjectM V S L Pavan Kuma 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.