Nutrartis S.A.

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

Refusal charges, in plain English

• HEALTH C1 refused line

  Unauthorized nutrient content or health claim

  The label or labeling appeared to carry a nutrient content claim or health claim that is not authorized.

• 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.

• 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 Nutrartis S.A.

Is Nutrartis S.A. on an FDA import alert?

No listing for Nutrartis S.A. appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Chile page.

Has FDA refused shipments from Nutrartis S.A.?

Yes. FDA refused 1 shipment line from Nutrartis S.A. on April 18, 2019. The most recent, on April 18, 2019, 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 Nutrartis S.A.'s shipments?

The most frequent charges are HEALTH C (unauthorized nutrient content or health claim, 1 line) and NCONTACT (no u.s. adverse event contact on supplement label, 1 line).

What is Nutrartis S.A.'s FEI number?

Nutrartis S.A.'s FDA Establishment Identifier (FEI) is 3013961077.