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Rudra Exim

FDA import alert and refusal historyGuntur, IndiaFEI 3043173511

Recorded by FDA as RUDRA EXIM

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Example subjectRudra Exi added to Import Alert 16-129 (red list)

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As of October 25, 2026, Rudra Exim is not on any FDA import alert in SupplierRadar's records; FDA refused 4 of its shipment lines between September 29, 2026 and October 7, 2026, most often for poisonous or deleterious substance (ordinarily injurious) (POISONORD).

Data from FDA public records, last checked . Request a correction

Current status

Import alerts
Not listed
Last import refusal
Betel nut, in shell · UNSAFE ADD
Last warning letter
None found
Last inspection
None on record

Every FDA record for Rudra Exim

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

2026

  1. Import refusal
    Refused, 3 lines in one entry: Betel nut, in shellUNSAFE ADDPOISONORDEntry DP4-8687034-9Show 3 lines
    Source
  2. Import refusal
    Refused, Pepper,black, whole (spice)FILTHYSALMONELLAEntry DP4-8687034-9
    Source

Refusal charges, in plain English

  • POISONORD3 refused lines

    Poisonous or deleterious substance (ordinarily injurious)

    The product appeared to contain a poisonous or deleterious substance in a form or amount that would ordinarily render it injurious to health.

  • UNSAFE ADD3 refused lines

    Food additive unsafe under section 409

    The product appeared to contain a food additive that is unsafe within the meaning of section 409 of the FD&C Act, the section that governs which food additives may be used and under what conditions.

  • 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.

  • SALMONELLA1 refused line

    Salmonella

    The product appeared to contain Salmonella, which the law treats as a poisonous and deleterious substance that may make food injurious to health.

Questions about Rudra Exim

Is Rudra Exim on an FDA import alert?
No listing for Rudra Exim appears in the FDA import alerts SupplierRadar checked on October 25, 2026. Country-wide alerts may still apply to its products; see the India page.
Has FDA refused shipments from Rudra Exim?
Yes. FDA refused 4 shipment lines from Rudra Exim between September 29, 2026 and October 7, 2026. The most recent, on October 7, 2026, was betel nut, in shell, charged as UNSAFE ADD (food additive unsafe under section 409).
Why did FDA refuse Rudra Exim's shipments?
The most frequent charges are POISONORD (poisonous or deleterious substance (ordinarily injurious), 3 lines) and UNSAFE ADD (food additive unsafe under section 409, 3 lines).
What is Rudra Exim's FEI number?
Rudra Exim's FDA Establishment Identifier (FEI) is 3043173511.

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Example subjectRudra Exi 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.