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SanPharma GmbH

FDA import alert and refusal historyHamburg, GermanyFEI 3007520191

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Example subjectSanPharma Gmb added to Import Alert 16-129 (red list)

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As of October 26, 2026, SanPharma GmbH is not on any FDA import alert in SupplierRadar's records; FDA refused 13 of its shipment lines on January 23, 2018, most often for required label information not in english (NO ENGLISH).

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

Current status

Import alerts
Not listed
Last import refusal
Vitamin, n.e.c. · NO ENGLISH
Last warning letter
None found
Last inspection
None on record

Every FDA record for SanPharma GmbH

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

2018

  1. Import refusal
    Refused, 13 lines in one entry: Vitamin, n.e.c.; Vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c.NO ENGLISHUNAPPROVEDEntry UPS-6733596-9Show 13 lines
    Source

Refusal charges, in plain English

  • NO ENGLISH13 refused lines

    Required label information not in English

    Information that must appear on the label appeared not to be given in English, or not to be repeated in every language used on the label.

  • UNAPPROVED4 refused lines

    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 SanPharma GmbH

Is SanPharma GmbH on an FDA import alert?
No listing for SanPharma 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 SanPharma GmbH?
Yes. FDA refused 13 shipment lines from SanPharma GmbH on January 23, 2018. The most recent, on January 23, 2018, was vitamin, n.e.c., charged as NO ENGLISH (required label information not in english).
Why did FDA refuse SanPharma GmbH's shipments?
The most frequent charges are NO ENGLISH (required label information not in english, 13 lines) and UNAPPROVED (unapproved new drug, 4 lines).
What is SanPharma GmbH's FEI number?
SanPharma GmbH's FDA Establishment Identifier (FEI) is 3007520191.

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Example subjectSanPharma 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.