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Bioprobif Saglik

FDA import alert and refusal historyMaltepe, TurkeyFEI 3035479598

Recorded by FDA as BIOPROBIF SAGLIK

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Example subjectBioprobif Sagli added to Import Alert 16-129 (red list)

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As of October 26, 2026, Bioprobif Saglik is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on August 11, 2025, 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
None on record

Every FDA record for Bioprobif Saglik

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

2025

  1. Import refusal
    Refused, Vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c.NCONTACTNUTRIT LBLEntry SCS-1586362-9
    Source

Refusal charges, in plain English

  • NCONTACT1 refused line

    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.

  • NUTRIT LBL1 refused line

    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 Bioprobif Saglik

Is Bioprobif Saglik on an FDA import alert?
No listing for Bioprobif Saglik appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Turkey page.
Has FDA refused shipments from Bioprobif Saglik?
Yes. FDA refused 1 shipment line from Bioprobif Saglik on August 11, 2025. The most recent, on August 11, 2025, 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 Bioprobif Saglik's shipments?
The most frequent charges are NCONTACT (no u.s. adverse event contact on supplement label, 1 line) and NUTRIT LBL (nutrition information missing from label, 1 line).
What is Bioprobif Saglik's FEI number?
Bioprobif Saglik's FDA Establishment Identifier (FEI) is 3035479598.

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Example subjectBioprobif Sagli 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.