SupplierRadar

Kringle Pharma

FDA import alert and refusal historyToyonaka, JapanFEI 3005459784

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Example subjectKringle Pharm added to Import Alert 16-129 (red list)

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As of October 26, 2026, Kringle Pharma is not on any FDA import alert in SupplierRadar's records; FDA refused 2 of its shipment lines on December 15, 2021, 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 Kringle Pharma

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

2021

  1. Import refusal
    Refused, 2 lines in one entry: Vitamin e (tocopherol)UNAPPROVEDEntry 799-6485102-5Show 2 lines
    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.

Questions about Kringle Pharma

Is Kringle Pharma on an FDA import alert?
No listing for Kringle Pharma appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Japan page.
Has FDA refused shipments from Kringle Pharma?
Yes. FDA refused 2 shipment lines from Kringle Pharma on December 15, 2021. The most recent, on December 15, 2021, was vitamin e (tocopherol), charged as UNAPPROVED (unapproved new drug).
Why did FDA refuse Kringle Pharma's shipments?
The most frequent charge is UNAPPROVED (unapproved new drug, 2 lines).
What is Kringle Pharma's FEI number?
Kringle Pharma's FDA Establishment Identifier (FEI) is 3005459784.

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Example subjectKringle Pharm 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.