Gueldenkron Fruchtsaft GmbH

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

Refusal charges, in plain English

• INADPRCCTL2 refused lines

  Inadequate process controls

  The product appeared to have been prepared, packed, or held under insanitary conditions because of inadequate process controls, whereby it may have become contaminated or injurious to health.

Questions about Gueldenkron Fruchtsaft GmbH

Is Gueldenkron Fruchtsaft GmbH on an FDA import alert?

Yes. As of October 26, 2026, Gueldenkron Fruchtsaft GmbH is on the red list of FDA Import Alert 99-38, “Low-acid canned/acidified foods: inadequate process control”, for ready to eat; shelf-stable; cold brew coffee; FDA published the listing on September 19, 2025.

Has FDA refused shipments from Gueldenkron Fruchtsaft GmbH?

Yes. FDA refused 2 shipment lines from Gueldenkron Fruchtsaft GmbH between November 17, 2025 and November 24, 2025. The most recent, on November 24, 2025, was coffee drink, charged as INADPRCCTL (inadequate process controls).

Why did FDA refuse Gueldenkron Fruchtsaft GmbH's shipments?

The most frequent charge is INADPRCCTL (inadequate process controls, 2 lines).

When was Gueldenkron Fruchtsaft GmbH last inspected by FDA?

FDA's most recent inspection of Gueldenkron Fruchtsaft GmbH with a final classification is dated May 28, 2025 and was classified OAI (Official Action Indicated).

What is Gueldenkron Fruchtsaft GmbH's FEI number?

Gueldenkron Fruchtsaft GmbH's FDA Establishment Identifier (FEI) is 3004650357.

Can shipments from Gueldenkron Fruchtsaft GmbH still enter the U.S.?

Shipments of ready to eat; shelf-stable; cold brew coffee from Gueldenkron Fruchtsaft GmbH can be detained without physical examination under Import Alert 99-38; FDA releases them only if evidence shows they do not have the listed violation. Importers must consider this listing in their FSVP evaluation (21 CFR 1.505).