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Abiogen Pharma Spa

FDA import alert and refusal historyOspedaletto, ItalyFEI 3005465066

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Example subjectAbiogen Pharma Sp added to Import Alert 16-129 (red list)

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As of October 26, 2026, Abiogen Pharma Spa is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on September 16, 2024, 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
Vitamin d2 (calciferol) · UNAPPROVED
Last warning letter
None found
Last inspection
None on record

Every FDA record for Abiogen Pharma Spa

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

2024

  1. Import refusal
    Refused, Vitamin d2 (calciferol)UNAPPROVEDEntry 799-3173833-1
    Source

Refusal charges, in plain English

  • UNAPPROVED1 refused line

    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 Abiogen Pharma Spa

Is Abiogen Pharma Spa on an FDA import alert?
No listing for Abiogen Pharma Spa appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Italy page.
Has FDA refused shipments from Abiogen Pharma Spa?
Yes. FDA refused 1 shipment line from Abiogen Pharma Spa on September 16, 2024. The most recent, on September 16, 2024, was vitamin d2 (calciferol), charged as UNAPPROVED (unapproved new drug).
Why did FDA refuse Abiogen Pharma Spa's shipments?
The most frequent charge is UNAPPROVED (unapproved new drug, 1 line).
What is Abiogen Pharma Spa's FEI number?
Abiogen Pharma Spa's FDA Establishment Identifier (FEI) is 3005465066.

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Example subjectAbiogen Pharma Sp 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.