SupplierRadar

W Medical Systems

FDA import alert and refusal historyLauenforde, GermanyFEI 3014096012

Recorded by FDA as W MEDICAL SYSTEMS

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Example subjectW Medical System added to Import Alert 16-129 (red list)

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As of October 26, 2026, W Medical Systems is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on April 20, 2022, most often for unapproved new drug (UNAPPROVED).

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

Current status

Import alerts
Not listed
Last import refusal
Cumin, ground, cracked (spice) · UNAPPROVED
Last warning letter
None found
Last inspection
None on record

Every FDA record for W Medical Systems

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

2022

  1. Import refusal
    Refused, Cumin, ground, cracked (spice)UNAPPROVEDEntry AEK-0941388-9
    Source

Refusal charges, in plain English

  • 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 W Medical Systems

Is W Medical Systems on an FDA import alert?
No listing for W Medical Systems 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 W Medical Systems?
Yes. FDA refused 1 shipment line from W Medical Systems on April 20, 2022. The most recent, on April 20, 2022, was cumin, ground, cracked (spice), charged as UNAPPROVED (unapproved new drug).
Why did FDA refuse W Medical Systems's shipments?
The most frequent charge is UNAPPROVED (unapproved new drug, 1 line).
What is W Medical Systems's FEI number?
W Medical Systems's FDA Establishment Identifier (FEI) is 3014096012.

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Example subjectW Medical System added to Import Alert 16-129 (red list)

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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.