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Sincrofarm, S.L.

FDA import alert and refusal historyCornella De Llobregat, SpainFEI 3012961202

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Example subjectSincrofarm, S.L added to Import Alert 16-129 (red list)

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As of October 26, 2026, Sincrofarm, S.L. is not on any FDA import alert in SupplierRadar's records; FDA refused 12 of its shipment lines between June 26, 2019 and November 24, 2020, most often for no u.s. adverse event contact on supplement label (NCONTACT).

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

Current status

Import alerts
Not listed
Last import refusal
Vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c. · NCONTACT
Last warning letter
None found
Last inspection
Classified NAI (No Action Indicated)

Every FDA record for Sincrofarm, S.L.

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

2025

  1. Inspection
    Inspection classified NAI (No Action Indicated)Food Composition, Standards, Labeling and Econ; Foodborne Biological Hazards
    Source

2020

  1. Import refusal
    Refused, 6 lines in one entry: Vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c.NCONTACTEntry 799-7990739-9Show 6 lines
    • Refused, Vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c.NCONTACTEntry 799-7990739-9Source
    • Refused, Vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c.NCONTACTEntry 799-7990739-9Source
    • Refused, Vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c.NCONTACTEntry 799-7990739-9Source
    • Refused, Vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c.NCONTACTEntry 799-7990739-9Source
    • Refused, Vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c.NCONTACTEntry 799-7990739-9Source
    • Refused, Vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c.NCONTACTEntry 799-7990739-9Source
    Source

2019

  1. Import refusal
    Refused, 2 lines in one entry: Dietary conventional foods, n.e.c.DIETARYLBLNO ENGLISHNUTRIT LBLEntry 799-3174799-0Show 2 lines
    Source
  2. Import refusal
    Refused, 4 lines in one entry: Manganese (mineral)COLORLABELDIETARYLBLNO ENGLISHEntry 799-1725753-5Show 4 lines
    Source

Refusal charges, in plain English

  • NCONTACT6 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.

  • COLORLABEL3 refused lines

    Required information not prominent

    Information required on the label appeared not to be placed prominently enough, or in such terms, to be read and understood by an ordinary consumer.

  • 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).

  • NO ENGLISH2 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 LBL2 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.

Questions about Sincrofarm, S.L.

Is Sincrofarm, S.L. on an FDA import alert?
No listing for Sincrofarm, S.L. appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Spain page.
Has FDA refused shipments from Sincrofarm, S.L.?
Yes. FDA refused 12 shipment lines from Sincrofarm, S.L. between June 26, 2019 and November 24, 2020. The most recent, on November 24, 2020, was vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c., charged as NCONTACT (no u.s. adverse event contact on supplement label).
Why did FDA refuse Sincrofarm, S.L.'s shipments?
The most frequent charges are NCONTACT (no u.s. adverse event contact on supplement label, 6 lines) and COLORLABEL (required information not prominent, 3 lines).
When was Sincrofarm, S.L. last inspected by FDA?
FDA's most recent inspection of Sincrofarm, S.L. with a final classification is dated February 17, 2025 and was classified NAI (No Action Indicated).
What is Sincrofarm, S.L.'s FEI number?
Sincrofarm, S.L.'s FDA Establishment Identifier (FEI) is 3012961202.

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Example subjectSincrofarm, S.L 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.