Is Fortitech Europe Aps on an FDA import alert?

No listing for Fortitech Europe Aps appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Denmark page.

Has FDA refused shipments from Fortitech Europe Aps?

No FDA import refusals for Fortitech Europe Aps appear in FDA's refusal data since October 2016, as of October 26, 2026.

When was Fortitech Europe Aps last inspected by FDA?

FDA's most recent inspection of Fortitech Europe Aps with a final classification is dated September 17, 2013 and was classified VAI (Voluntary Action Indicated).

What is Fortitech Europe Aps's FEI number?

Fortitech Europe Aps's FDA Establishment Identifier (FEI) is 3005250381.

Fortitech Europe Aps

FDA import alert and refusal historyGadstrup, DenmarkFEI 3005250381

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As of October 26, 2026, Fortitech Europe Aps has no FDA import alert listing or import refusal in SupplierRadar's records; its most recent FDA inspection, on September 17, 2013, was classified VAI (Voluntary Action Indicated).

Data from FDA public records, last checked October 26, 2026. Request a correction

Current status

Import alerts: Not listed
Last import refusal: None since October 2016
Last warning letter: None found
Last inspection: Sep 17, 2013Classified VAI (Voluntary Action Indicated)

Every FDA record for Fortitech Europe Aps

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

2013

Sep 17, 2013Inspection
Inspection classified VAI (Voluntary Action Indicated)Food Composition, Standards, Labeling and Econ
Source

2011

Aug 30, 2011Inspection
Inspection classified NAI (No Action Indicated)Food Composition, Standards, Labeling and Econ
Source

2010

Jul 14, 2010Inspection
Inspection classified NAI (No Action Indicated)Food Composition, Standards, Labeling and Econ
Source

Questions about Fortitech Europe Aps

Is Fortitech Europe Aps on an FDA import alert?: No listing for Fortitech Europe Aps appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Denmark page.
Has FDA refused shipments from Fortitech Europe Aps?: No FDA import refusals for Fortitech Europe Aps appear in FDA's refusal data since October 2016, as of October 26, 2026.
When was Fortitech Europe Aps last inspected by FDA?: FDA's most recent inspection of Fortitech Europe Aps with a final classification is dated September 17, 2013 and was classified VAI (Voluntary Action Indicated).
What is Fortitech Europe Aps's FEI number?: Fortitech Europe Aps's FDA Establishment Identifier (FEI) is 3005250381.

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SupplierRadar is not affiliated with the U.S. Food and Drug Administration. Data comes from public FDA records and may contain errors. This is not legal advice; importers remain responsible for their supplier evaluations.