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Dragenopharm Apotheker Pueschl GmbH

FDA import alert and refusal historyTittmoning, GermanyFEI 3009943598

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Example subjectDragenopharm Apotheker Pueschl Gmb added to Import Alert 16-129 (red list)

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As of October 27, 2026, Dragenopharm Apotheker Pueschl GmbH is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on October 2, 2020, 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
Mint (herbal & botanicals, not teas - if tea form see 31p) · UNAPPROVED
Last warning letter
None found
Last inspection
Classified VAI (Voluntary Action Indicated)

Every FDA record for Dragenopharm Apotheker Pueschl GmbH

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

2020

  1. Import refusal
    Refused, Mint (herbal & botanicals, not teas - if tea form see 31p)UNAPPROVEDEntry 799-8532443-1
    Source

2017

  1. Inspection
    Inspection classified VAI (Voluntary Action Indicated)Food Composition, Standards, Labeling and Econ
    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 Dragenopharm Apotheker Pueschl GmbH

Is Dragenopharm Apotheker Pueschl GmbH on an FDA import alert?
No listing for Dragenopharm Apotheker Pueschl GmbH appears in the FDA import alerts SupplierRadar checked on October 27, 2026. Country-wide alerts may still apply to its products; see the Germany page.
Has FDA refused shipments from Dragenopharm Apotheker Pueschl GmbH?
Yes. FDA refused 1 shipment line from Dragenopharm Apotheker Pueschl GmbH on October 2, 2020. The most recent, on October 2, 2020, was mint (herbal & botanicals, not teas - if tea form see 31p), charged as UNAPPROVED (unapproved new drug).
Why did FDA refuse Dragenopharm Apotheker Pueschl GmbH's shipments?
The most frequent charge is UNAPPROVED (unapproved new drug, 1 line).
When was Dragenopharm Apotheker Pueschl GmbH last inspected by FDA?
FDA's most recent inspection of Dragenopharm Apotheker Pueschl GmbH with a final classification is dated May 19, 2017 and was classified VAI (Voluntary Action Indicated).
What is Dragenopharm Apotheker Pueschl GmbH's FEI number?
Dragenopharm Apotheker Pueschl GmbH's FDA Establishment Identifier (FEI) is 3009943598.

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Example subjectDragenopharm Apotheker Pueschl Gmb 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.