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Le Bouake Company

FDA import alert and refusal historyAbidjan, Cote d'IvoireFEI 3017968066

Recorded by FDA as LE BOUAKE COMPANY

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Example subjectLe Bouake Compan added to Import Alert 16-129 (red list)

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As of October 26, 2026, Le Bouake Company is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on October 15, 2020, 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
Herbals & botanical teas, n.e.c. · UNAPPROVED
Last warning letter
None found
Last inspection
None on record

Every FDA record for Le Bouake Company

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

2020

  1. Import refusal
    Refused, Herbals & botanical teas, n.e.c.UNAPPROVEDEntry CCT-0985432-2
    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 Le Bouake Company

Is Le Bouake Company on an FDA import alert?
No listing for Le Bouake Company appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Cote d'Ivoire page.
Has FDA refused shipments from Le Bouake Company?
Yes. FDA refused 1 shipment line from Le Bouake Company on October 15, 2020. The most recent, on October 15, 2020, was herbals & botanical teas, n.e.c., charged as UNAPPROVED (unapproved new drug).
Why did FDA refuse Le Bouake Company's shipments?
The most frequent charge is UNAPPROVED (unapproved new drug, 1 line).
What is Le Bouake Company's FEI number?
Le Bouake Company's FDA Establishment Identifier (FEI) is 3017968066.

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Example subjectLe Bouake Compan 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.