SupplierRadar

Hawa Sannoh

FDA import alert and refusal historyBushrod Island, LiberiaFEI 3048796546

Recorded by FDA as HAWA SANNOH

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Example subjectHawa Sanno added to Import Alert 16-129 (red list)

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As of October 26, 2026, Hawa Sannoh is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on October 9, 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
Citrus aurantium ( herbal & botanical other than teas) · UNAPPROVED
Last warning letter
None found
Last inspection
None on record

Every FDA record for Hawa Sannoh

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

2026

  1. Import refusal
    Refused, Citrus aurantium ( herbal & botanical other than teas)UNAPPROVEDEntry AEK-2288696-3
    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 Hawa Sannoh

Is Hawa Sannoh on an FDA import alert?
No listing for Hawa Sannoh appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Liberia page.
Has FDA refused shipments from Hawa Sannoh?
Yes. FDA refused 1 shipment line from Hawa Sannoh on October 9, 2026. The most recent, on October 9, 2026, was citrus aurantium ( herbal & botanical other than teas), charged as UNAPPROVED (unapproved new drug).
Why did FDA refuse Hawa Sannoh's shipments?
The most frequent charge is UNAPPROVED (unapproved new drug, 1 line).
What is Hawa Sannoh's FEI number?
Hawa Sannoh's FDA Establishment Identifier (FEI) is 3048796546.

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Example subjectHawa Sanno 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.