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Bee Bite

FDA import alert and refusal historySaldus, LatviaFEI 3025986460

Recorded by FDA as BEE BITE

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Example subjectBee Bit added to Import Alert 16-129 (red list)

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As of October 26, 2026, Bee Bite is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on November 1, 2024, 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
Bee pollen (vit/min/protein/unconventional dietary spec for human/animal, n.e.c.) · UNAPPROVED
Last warning letter
None found
Last inspection
None on record

Every FDA record for Bee Bite

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

2024

  1. Import refusal
    Refused, Bee pollen (vit/min/protein/unconventional dietary spec for human/animal, n.e.c.)UNAPPROVEDEntry AEK-6520862-9
    Source

Refusal charges, in plain English

  • UNAPPROVED1 refused line

    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 Bee Bite

Is Bee Bite on an FDA import alert?
No listing for Bee Bite appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Latvia page.
Has FDA refused shipments from Bee Bite?
Yes. FDA refused 1 shipment line from Bee Bite on November 1, 2024. The most recent, on November 1, 2024, was bee pollen (vit/min/protein/unconventional dietary spec for human/animal, n.e.c.), charged as UNAPPROVED (unapproved new drug).
Why did FDA refuse Bee Bite's shipments?
The most frequent charge is UNAPPROVED (unapproved new drug, 1 line).
What is Bee Bite's FEI number?
Bee Bite's FDA Establishment Identifier (FEI) is 3025986460.

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Example subjectBee Bit 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.