SupplierRadar

Teofarma S R L

FDA import alert and refusal historyTorrevecchia Pia, ItalyFEI 3012771530

Recorded by FDA as TEOFARMA S R L

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

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As of October 26, 2026, Teofarma S R L is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on July 5, 2017, 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
Antioxidants (food additives for human use) · UNAPPROVED
Last warning letter
None found
Last inspection
None on record

Every FDA record for Teofarma S R L

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

2017

  1. Import refusal
    Refused, Antioxidants (food additives for human use)UNAPPROVEDEntry AEK-3634770-3
    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 Teofarma S R L

Is Teofarma S R L on an FDA import alert?
No listing for Teofarma S R L 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 Teofarma S R L?
Yes. FDA refused 1 shipment line from Teofarma S R L on July 5, 2017. The most recent, on July 5, 2017, was antioxidants (food additives for human use), charged as UNAPPROVED (unapproved new drug).
Why did FDA refuse Teofarma S R L's shipments?
The most frequent charge is UNAPPROVED (unapproved new drug, 1 line).
What is Teofarma S R L's FEI number?
Teofarma S R L's FDA Establishment Identifier (FEI) is 3012771530.

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Example subjectTeofarma S R 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.