SupplierRadar

Jigsimur SA

FDA import alert and refusal historyWestern Cape, Saudi ArabiaFEI 3028983571

Recorded by FDA as JIGSIMUR SA

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Example subjectJigsimur S added to Import Alert 16-129 (red list)

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As of October 26, 2026, Jigsimur SA is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on September 26, 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
Aloe (herbal and botanical (not teas) ii (continued)) · UNAPPROVED
Last warning letter
None found
Last inspection
None on record

Every FDA record for Jigsimur SA

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

2024

  1. Import refusal
    Refused, Aloe (herbal and botanical (not teas) ii (continued))UNAPPROVEDEntry AR8-2023130-6
    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 Jigsimur SA

Is Jigsimur SA on an FDA import alert?
No listing for Jigsimur SA appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Saudi Arabia page.
Has FDA refused shipments from Jigsimur SA?
Yes. FDA refused 1 shipment line from Jigsimur SA on September 26, 2024. The most recent, on September 26, 2024, was aloe (herbal and botanical (not teas) ii (continued)), charged as UNAPPROVED (unapproved new drug).
Why did FDA refuse Jigsimur SA's shipments?
The most frequent charge is UNAPPROVED (unapproved new drug, 1 line).
What is Jigsimur SA's FEI number?
Jigsimur SA's FDA Establishment Identifier (FEI) is 3028983571.

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Example subjectJigsimur S 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.