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Synoptis Pharma Sp

FDA import alert and refusal historyWarsaw, PolandFEI 3014672004

Recorded by FDA as SYNOPTIS PHARMA SP

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

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As of October 26, 2026, Synoptis Pharma Sp is not on any FDA import alert in SupplierRadar's records; FDA refused 14 of its shipment lines between November 4, 2020 and April 14, 2023, most often for required label information not in english (NO ENGLISH).

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

Current status

Import alerts
Not listed
Last import refusal
Herbals & botanicals (not teas), n.e.c. · NO ENGLISH
Last warning letter
None found
Last inspection
None on record

Every FDA record for Synoptis Pharma Sp

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

2023

  1. Import refusal
    Refused, 9 lines in one entry: Herbals & botanicals (not teas), n.e.c.NO ENGLISHEntry 799-4290878-1Show 9 lines
    Source
  2. Import refusal
    Refused, Vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c.LIST INGRENO ENGLISHLABELINGEntry 799-4201207-1
    Source

2021

  1. Import refusal
    Refused, 2 lines in one entry: Vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c.NO ENGLISHNCONTACTNUTRIT LBLEntry 799-5959324-4Show 2 lines
    Source

2020

  1. Import refusal
    Refused, 2 lines in one entry: Vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c.DIETARYLBLNO ENGLISHNUTRIT LBLEntry 799-8284934-9Show 2 lines
    Source

Refusal charges, in plain English

  • NO ENGLISH14 refused lines

    Required label information not in English

    Information that must appear on the label appeared not to be given in English, or not to be repeated in every language used on the label.

  • NUTRIT LBL4 refused lines

    Nutrition information missing from label

    The label or labeling appeared not to carry the nutrition information that U.S. law requires for the food.

  • DIETARYLBL2 refused lines

    Not identified as a dietary supplement

    The label appeared not to identify the product with the term "dietary supplement" (which may be modified with the name of an ingredient).

  • NCONTACT2 refused lines

    No U.S. adverse event contact on supplement label

    The dietary supplement label appeared not to show a U.S. address or phone number through which a serious adverse event can be reported.

  • LABELING1 refused line

    Fair Packaging and Labeling Act

    The package appeared not to meet the Fair Packaging and Labeling Act because of the placement, form, or contents of a required label statement.

  • LIST INGRE1 refused line

    Ingredients not listed

    The product is made from two or more ingredients and the label appeared not to list the common or usual name of each one (or, for a juice beverage, the percentage of juice).

Questions about Synoptis Pharma Sp

Is Synoptis Pharma Sp on an FDA import alert?
No listing for Synoptis Pharma Sp 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 Synoptis Pharma Sp?
Yes. FDA refused 14 shipment lines from Synoptis Pharma Sp between November 4, 2020 and April 14, 2023. The most recent, on April 14, 2023, was herbals & botanicals (not teas), n.e.c., charged as NO ENGLISH (required label information not in english).
Why did FDA refuse Synoptis Pharma Sp's shipments?
The most frequent charges are NO ENGLISH (required label information not in english, 14 lines) and NUTRIT LBL (nutrition information missing from label, 4 lines).
What is Synoptis Pharma Sp's FEI number?
Synoptis Pharma Sp's FDA Establishment Identifier (FEI) is 3014672004.

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Example subjectSynoptis Pharma 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.