Sela Tasimacilik Ic Ve Dis Ticaret

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

Refusal charges, in plain English

• UNAPPROVED5 refused lines

  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.

• UNSAFE ADD4 refused lines

  Food additive unsafe under section 409

  The product appeared to contain a food additive that is unsafe within the meaning of section 409 of the FD&C Act, the section that governs which food additives may be used and under what conditions.

• POISONOUS1 refused line

  Poisonous or deleterious substance

  The product appeared to bear or contain a poisonous or deleterious substance which may render it injurious to health.

Questions about Sela Tasimacilik Ic Ve Dis Ticaret

Is Sela Tasimacilik Ic Ve Dis Ticaret on an FDA import alert?

No listing for Sela Tasimacilik Ic Ve Dis Ticaret 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 Sela Tasimacilik Ic Ve Dis Ticaret?

Yes. FDA refused 10 shipment lines from Sela Tasimacilik Ic Ve Dis Ticaret between August 13, 2021 and February 22, 2023. The most recent, on February 22, 2023, was royal jelly (vit/min/protein/unconventional dietary spec for human/animal, n.e.c.), charged as UNAPPROVED (unapproved new drug).

Why did FDA refuse Sela Tasimacilik Ic Ve Dis Ticaret's shipments?

The most frequent charges are UNAPPROVED (unapproved new drug, 5 lines) and UNSAFE ADD (food additive unsafe under section 409, 4 lines).

What is Sela Tasimacilik Ic Ve Dis Ticaret's FEI number?

Sela Tasimacilik Ic Ve Dis Ticaret's FDA Establishment Identifier (FEI) is 3019677660.