SupplierRadar

Jla Pty Ltd

FDA import alert and refusal historyKnysna, South AfricaFEI 3013268104

Recorded by FDA as JLA PTY LTD

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Example subjectJla Pty Lt added to Import Alert 16-129 (red list)

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As of October 26, 2026, Jla Pty Ltd is not on any FDA import alert in SupplierRadar's records; FDA refused 2 of its shipment lines on April 26, 2019, 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
Tea, green · UNAPPROVED
Last warning letter
None found
Last inspection
None on record

Every FDA record for Jla Pty Ltd

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

2019

  1. Import refusal
    Refused, Tea, greenUNAPPROVEDEntry AEK-5776125-3
    Source
  2. Import refusal
    Refused, Tea, greenUNAPPROVEDEntry AEK-5783295-5
    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 Jla Pty Ltd

Is Jla Pty Ltd on an FDA import alert?
No listing for Jla Pty Ltd appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the South Africa page.
Has FDA refused shipments from Jla Pty Ltd?
Yes. FDA refused 2 shipment lines from Jla Pty Ltd on April 26, 2019. The most recent, on April 26, 2019, was tea, green, charged as UNAPPROVED (unapproved new drug).
Why did FDA refuse Jla Pty Ltd's shipments?
The most frequent charge is UNAPPROVED (unapproved new drug, 2 lines).
What is Jla Pty Ltd's FEI number?
Jla Pty Ltd's FDA Establishment Identifier (FEI) is 3013268104.

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Example subjectJla Pty Lt 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.