Ayanda GmbH

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

Refusal charges, in plain English

• 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 Ayanda GmbH

Is Ayanda GmbH on an FDA import alert?

No listing for Ayanda GmbH 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 Ayanda GmbH?

Yes. FDA refused 1 shipment line from Ayanda GmbH on July 25, 2025. The most recent, on July 25, 2025, was 54k[][]22/turmeric (herbal & botanicals, not teas ii), charged as NOT LISTED (product not listed with fda).

Why did FDA refuse Ayanda GmbH's shipments?

The most frequent charges are NOT LISTED (product not listed with fda, 1 line) and UNAPPROVED (unapproved new drug, 1 line).

When was Ayanda GmbH last inspected by FDA?

FDA's most recent inspection of Ayanda GmbH with a final classification is dated April 3, 2019 and was classified VAI (Voluntary Action Indicated).

What is Ayanda GmbH's FEI number?

Ayanda GmbH's FDA Establishment Identifier (FEI) is 3009926968.