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Sanivarapu Revathi

FDA import alert and refusal historyNarasaraopet, IndiaFEI 3045500482

Recorded by FDA as SANIVARAPU REVATHI

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Example subjectSanivarapu Revath added to Import Alert 16-129 (red list)

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As of October 26, 2026, Sanivarapu Revathi is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on August 26, 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
Other bakery products, n.e.c. · FILTHY
Last warning letter
None found
Last inspection
None on record

Every FDA record for Sanivarapu Revathi

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

2026

  1. Import refusal
    Refused, Other bakery products, n.e.c.FILTHYEntry SCS-2989532-1
    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 Sanivarapu Revathi

Is Sanivarapu Revathi on an FDA import alert?
No listing for Sanivarapu Revathi 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 Sanivarapu Revathi?
Yes. FDA refused 1 shipment line from Sanivarapu Revathi on August 26, 2026. The most recent, on August 26, 2026, was other bakery products, n.e.c., charged as FILTHY (filthy, putrid or decomposed substance).
Why did FDA refuse Sanivarapu Revathi's shipments?
The most frequent charge is FILTHY (filthy, putrid or decomposed substance, 1 line).
What is Sanivarapu Revathi's FEI number?
Sanivarapu Revathi's FDA Establishment Identifier (FEI) is 3045500482.

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Example subjectSanivarapu Revath 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.