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Pendyala Chandrakala

FDA import alert and refusal historyHyderabad, IndiaFEI 3046051678

Recorded by FDA as PENDYALA CHANDRAKALA

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Example subjectPendyala Chandrakal added to Import Alert 16-129 (red list)

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As of October 26, 2026, Pendyala Chandrakala is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on September 24, 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 Pendyala Chandrakala

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

2026

  1. Import refusal
    Refused, Tamarind, dried or pasteFILTHYEntry SCS-1904057-3
    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 Pendyala Chandrakala

Is Pendyala Chandrakala on an FDA import alert?
No listing for Pendyala Chandrakala 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 Pendyala Chandrakala?
Yes. FDA refused 1 shipment line from Pendyala Chandrakala on September 24, 2026. The most recent, on September 24, 2026, was tamarind, dried or paste, charged as FILTHY (filthy, putrid or decomposed substance).
Why did FDA refuse Pendyala Chandrakala's shipments?
The most frequent charge is FILTHY (filthy, putrid or decomposed substance, 1 line).
What is Pendyala Chandrakala's FEI number?
Pendyala Chandrakala's FDA Establishment Identifier (FEI) is 3046051678.

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Example subjectPendyala Chandrakal 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.