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Tulip Iternational Inc.

FDA import alert and refusal historySeoul, South KoreaFEI 3012558840

Recorded by FDA as TULIP ITERNATIONAL INC.

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Example subjectTulip Iternational Inc added to Import Alert 16-129 (red list)

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As of October 26, 2026, Tulip Iternational Inc. is not on any FDA import alert in SupplierRadar's records; FDA refused 2 of its shipment lines on January 26, 2017, most often for poisonous or deleterious substance (POISONOUS).

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

Current status

Import alerts
Not listed
Last import refusal
Tea, n.e.c. · POISONOUS
Last warning letter
None found
Last inspection
None on record

Every FDA record for Tulip Iternational Inc.

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

2017

  1. Import refusal
    Refused, 2 lines in one entry: Tea, n.e.c.POISONOUSEntry 9EH-0014192-1Show 2 lines
    Source

Refusal charges, in plain English

  • POISONOUS2 refused lines

    Poisonous or deleterious substance

    The product appeared to bear or contain a poisonous or deleterious substance which may render it injurious to health.

Questions about Tulip Iternational Inc.

Is Tulip Iternational Inc. on an FDA import alert?
No listing for Tulip Iternational Inc. appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the South Korea page.
Has FDA refused shipments from Tulip Iternational Inc.?
Yes. FDA refused 2 shipment lines from Tulip Iternational Inc. on January 26, 2017. The most recent, on January 26, 2017, was tea, n.e.c., charged as POISONOUS (poisonous or deleterious substance).
Why did FDA refuse Tulip Iternational Inc.'s shipments?
The most frequent charge is POISONOUS (poisonous or deleterious substance, 2 lines).
What is Tulip Iternational Inc.'s FEI number?
Tulip Iternational Inc.'s FDA Establishment Identifier (FEI) is 3012558840.

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Example subjectTulip Iternational Inc 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.