Previtalica e.K.

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

Refusal charges, in plain English

• FRNMFGREG1 refused line

  FRNMFGREG

• NOT LISTED1 refused line

  Product not listed with FDA

  The product appeared to be a drug or device that is not included in the listing FDA requires under section 510(j) of the FD&C Act.

• 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 Previtalica e.K.

Is Previtalica e.K. on an FDA import alert?

No listing for Previtalica e.K. appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Germany page.

Has FDA refused shipments from Previtalica e.K.?

Yes. FDA refused 1 shipment line from Previtalica e.K. on February 26, 2026. The most recent, on February 26, 2026, was nutrtionally incomplete formulations (protein, carbohydrate or fat modulars), charged as NOT LISTED (product not listed with fda).

Why did FDA refuse Previtalica e.K.'s shipments?

The most frequent charges are FRNMFGREG (frnmfgreg, 1 line) and NOT LISTED (product not listed with fda, 1 line).

What is Previtalica e.K.'s FEI number?

Previtalica e.K.'s FDA Establishment Identifier (FEI) is 3029798627.