SupplierRadar

Tymbark SA

FDA import alert and refusal historyTymbark, PolandFEI 3012335367

Recorded by FDA as TYMBARK SA

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

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As of October 26, 2026, Tymbark SA is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on September 11, 2024, most often for pesticide chemical residue (PESTICIDE).

Data from FDA public records, last checked . Request a correction

Current status

Import alerts
Not listed
Last import refusal
Orange, citrus fruit juices or concentrates · PESTICIDE
Last warning letter
None found
Last inspection
None on record

Every FDA record for Tymbark SA

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

2024

  1. Import refusal
    Refused, Orange, citrus fruit juices or concentratesPESTICIDEEntry 9AJ-0862357-9
    Source

Refusal charges, in plain English

  • PESTICIDE1 refused line

    Pesticide chemical residue

    The product appeared to contain a pesticide chemical residue that makes it adulterated under section 402(a)(2)(B) of the FD&C Act, for example a residue above the U.S. tolerance or one with no U.S. tolerance for that food.

Questions about Tymbark SA

Is Tymbark SA on an FDA import alert?
No listing for Tymbark SA appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Poland page.
Has FDA refused shipments from Tymbark SA?
Yes. FDA refused 1 shipment line from Tymbark SA on September 11, 2024. The most recent, on September 11, 2024, was orange, citrus fruit juices or concentrates, charged as PESTICIDE (pesticide chemical residue).
Why did FDA refuse Tymbark SA's shipments?
The most frequent charge is PESTICIDE (pesticide chemical residue, 1 line).
What is Tymbark SA's FEI number?
Tymbark SA's FDA Establishment Identifier (FEI) is 3012335367.

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Example subjectTymbark 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.