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Indo Rama Engg

FDA import alert and refusal historyPradesh, IndiaFEI 3017260281

Recorded by FDA as INDO RAMA ENGG

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Example subjectIndo Rama Eng added to Import Alert 16-129 (red list)

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As of October 25, 2026, Indo Rama Engg is not on any FDA import alert in SupplierRadar's records; FDA refused 2 of its shipment lines between September 16, 2026 and September 22, 2026, most often for unapproved new drug (UNAPPROVED).

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

Current status

Import alerts
Not listed
Last import refusal
Vitamin e (tocopherol) · UNAPPROVED
Last warning letter
None found
Last inspection
None on record

Every FDA record for Indo Rama Engg

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

2026

  1. Import refusal
    Refused, Vitamin e (tocopherol)UNAPPROVEDEntry AEK-9743642-0
    Source
  2. Import refusal
    Refused, Vitamin d2 (calciferol)NOT LISTEDUNAPPROVEDEntry AEK-9687524-8
    Source

Refusal charges, in plain English

  • UNAPPROVED2 refused lines

    Unapproved new drug

    The product appeared to be a new drug within the meaning of section 201(p) of the FD&C Act without an approved New Drug Application. FDA can apply this charge to a food or supplement whose labeling presents it for drug uses.

  • NOT LISTED1 refused line

    Product not listed with FDA

    The product appeared to be a drug or device that is not included in the listing FDA requires under section 510(j) of the FD&C Act.

Questions about Indo Rama Engg

Is Indo Rama Engg on an FDA import alert?
No listing for Indo Rama Engg 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 Indo Rama Engg?
Yes. FDA refused 2 shipment lines from Indo Rama Engg between September 16, 2026 and September 22, 2026. The most recent, on September 22, 2026, was vitamin e (tocopherol), charged as UNAPPROVED (unapproved new drug).
Why did FDA refuse Indo Rama Engg's shipments?
The most frequent charges are UNAPPROVED (unapproved new drug, 2 lines) and NOT LISTED (product not listed with fda, 1 line).
What is Indo Rama Engg's FEI number?
Indo Rama Engg's FDA Establishment Identifier (FEI) is 3017260281.

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Example subjectIndo Rama Eng 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.