Linden-Apotheke M. Spiegel 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

• NO ENGLISH1 refused line

  Required label information not in English

  Information that must appear on the label appeared not to be given in English, or not to be repeated in every language used on the label.

• 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 Linden-Apotheke M. Spiegel E.K.

Is Linden-Apotheke M. Spiegel E.K. on an FDA import alert?

No listing for Linden-Apotheke M. Spiegel 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 Linden-Apotheke M. Spiegel E.K.?

Yes. FDA refused 1 shipment line from Linden-Apotheke M. Spiegel E.K. on August 26, 2026. The most recent, on August 26, 2026, was vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c., charged as NOT LISTED (product not listed with fda).

Why did FDA refuse Linden-Apotheke M. Spiegel E.K.'s shipments?

The most frequent charges are FRNMFGREG (frnmfgreg, 1 line) and NO ENGLISH (required label information not in english, 1 line).

What is Linden-Apotheke M. Spiegel E.K.'s FEI number?

Linden-Apotheke M. Spiegel E.K.'s FDA Establishment Identifier (FEI) is 3015657400.