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Weleda AG

⚠️ High Risk

FEI: 1000326682 • Schwabisch Gmund, Baden-Wurttemberg • GERMANY

FEI

FEI Number

1000326682

📍

Location

Schwabisch Gmund, Baden-Wurttemberg

🇩🇪

Country

GERMANY
🏢

Address

Mohlerstr. 3-5, , Schwabisch Gmund, Baden-Wurttemberg, Germany

High Risk

FDA Import Risk Assessment

63.9
LowModerateHighCritical

This firm has a significant history of FDA import refusals with notable violations.

Statistics

26
Total Refusals
9
Unique Violations
1/28/2025
Latest Refusal
10/11/2001
Earliest Refusal

Score Breakdown

Violation Severity
76.7×40%
Refusal Volume
53.0×30%
Recency
80.9×20%
Frequency
11.2×10%
How is this score calculated?

Proprietary Algorithm

  • 40% Violation Severity — AI-assessed (1-10)
  • 30% Refusal Volume — Logarithmic scale
  • 20% Recency — Decays over 5 years
  • 10% Frequency — Refusals per year

© ImportRefusal.com Original Analysis

Violation Summary

7521×

UNAPPROVED

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be a new drug within the meaning of Section 201(p) without an approved New Drug Application (NDA).

276×

DRUG GMPS

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the methods used in and controls used for the manufacture, processing, packing, or holding of drugs and other products do not appear to conform to current good manufacturing practices within the meaning of Section 501(a)(2)(B).

1185×

NOT LISTED

It appears the drug or device is not included in a list required by Section 510(j), or a notice or other information respecting it was not provided as required by section 510(j) or 510(k).

162×

DIRECTIONS

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it is a device whose label appears to not bear adequate directions for use.

2231×

FALSE

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it is a device whose labeling appears to be false or misleading.

3241×

NO ENGLISH

The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of Section 403(f) of the FD&C Act in that any word, statement, or other information required by or under the authority of the FD&C Act to appear on the label or labeling is not prominently placed thereon with such conspicuousness (as compared with other words, statements, designs, or devices, in the labeling) and in such terms as to render it likely to be read and understood by the ordinary individual under customary terms of purchase and use (for example, label contains information in two or more languages but fails to repeat all required information in both languages in accordance with 21 CFR 101.15(c)(2), or label fails to include all required information in English in accordance with 21 CFR 101.15(c)(1), except in the case of articles distributed solely in the Commonwealth of Puerto Rico or in a Territory where the predominant language is one other than English)).

3311×

DR QUALITC

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the drug appears to be represented as not being recognized in an official compendium and appears its strength differs from or its quality or purity falls below, that which it purports or is represented to possess.

4711×

CSTIC LBLG

The labeling appears to fail to comply with cosmetic labeling requirements of Section 602(a), and/or (b), and/or (c), and as identified by 21 C.F.R. Part 701.

4721×

NO ENGLISH

Required label or labeling appears to not be in English in violation of 21 C.F.R. 201.15(c)(1).

Refusal History

DateProductViolationsDivision
1/28/2025
53AC02LOTIONS, OILS, POWDERS AND CREAMS (BABY PRODUCTS)
471CSTIC LBLG
Division of Southeast Imports (DSEI)
10/28/2011
66VIP99MISCELLANEOUS PATENT MEDICINES, ETC.
75UNAPPROVED
New Orleans District Office (NOL-DO)
10/17/2009
66VCP99MISCELLANEOUS PATENT MEDICINES, ETC.
27DRUG GMPS
75UNAPPROVED
New Orleans District Office (NOL-DO)
10/17/2009
66VCP99MISCELLANEOUS PATENT MEDICINES, ETC.
27DRUG GMPS
75UNAPPROVED
New Orleans District Office (NOL-DO)
10/17/2009
62GBL99ANTI-INFLAMMATORY N.E.C.
27DRUG GMPS
75UNAPPROVED
New Orleans District Office (NOL-DO)
10/6/2009
66VIP99MISCELLANEOUS PATENT MEDICINES, ETC.
27DRUG GMPS
75UNAPPROVED
New Orleans District Office (NOL-DO)
1/28/2008
54AYY99VITAMIN, N.E.C.
324NO ENGLISH
New Orleans District Office (NOL-DO)
9/14/2006
66VCY99MISCELLANEOUS PATENT MEDICINES, ETC.
118NOT LISTED
75UNAPPROVED
New York District Office (NYK-DO)
9/14/2006
66VCY99MISCELLANEOUS PATENT MEDICINES, ETC.
118NOT LISTED
75UNAPPROVED
New York District Office (NYK-DO)
9/14/2006
66VCY99MISCELLANEOUS PATENT MEDICINES, ETC.
118NOT LISTED
75UNAPPROVED
New York District Office (NYK-DO)
2/17/2005
62ICP99ANTI-NEOPLASTIC N.E.C.
75UNAPPROVED
New Orleans District Office (NOL-DO)
12/30/2004
66VAS99MISCELLANEOUS PATENT MEDICINES, ETC.
118NOT LISTED
16DIRECTIONS
New York District Office (NYK-DO)
10/29/2004
62FAB99ANTI-INFECTIVE, TOPICAL N.E.C.
331DR QUALITC
472NO ENGLISH
New Orleans District Office (NOL-DO)
5/20/2004
66VAC99MISCELLANEOUS PATENT MEDICINES, ETC.
16DIRECTIONS
27DRUG GMPS
New Orleans District Office (NOL-DO)
1/26/2004
66VBY99MISCELLANEOUS PATENT MEDICINES, ETC.
118NOT LISTED
75UNAPPROVED
Cincinnati District Office (CIN-DO)
8/16/2002
66VCK99MISCELLANEOUS PATENT MEDICINES, ETC.
75UNAPPROVED
New York District Office (NYK-DO)
8/16/2002
66VCK99MISCELLANEOUS PATENT MEDICINES, ETC.
75UNAPPROVED
New York District Office (NYK-DO)
8/16/2002
66VCK99MISCELLANEOUS PATENT MEDICINES, ETC.
75UNAPPROVED
New York District Office (NYK-DO)
8/16/2002
66VCK99MISCELLANEOUS PATENT MEDICINES, ETC.
75UNAPPROVED
New York District Office (NYK-DO)
8/16/2002
66VCK99MISCELLANEOUS PATENT MEDICINES, ETC.
75UNAPPROVED
New York District Office (NYK-DO)
8/16/2002
66VCK99MISCELLANEOUS PATENT MEDICINES, ETC.
75UNAPPROVED
New York District Office (NYK-DO)
8/16/2002
66VCK99MISCELLANEOUS PATENT MEDICINES, ETC.
75UNAPPROVED
New York District Office (NYK-DO)
8/16/2002
66VCK99MISCELLANEOUS PATENT MEDICINES, ETC.
75UNAPPROVED
New York District Office (NYK-DO)
8/16/2002
66VCK99MISCELLANEOUS PATENT MEDICINES, ETC.
75UNAPPROVED
New York District Office (NYK-DO)
8/16/2002
66VCK99MISCELLANEOUS PATENT MEDICINES, ETC.
75UNAPPROVED
New York District Office (NYK-DO)
10/11/2001
66VAY99MISCELLANEOUS PATENT MEDICINES, ETC.
223FALSE
27DRUG GMPS
75UNAPPROVED
New Orleans District Office (NOL-DO)

Frequently Asked Questions

What is Weleda AG's FDA import refusal history?

Weleda AG (FEI: 1000326682) has 26 FDA import refusal record(s) in our database, spanning from 10/11/2001 to 1/28/2025.

What is an FEI number?

FEI stands for Firm Establishment Identifier. It's a unique number assigned by the FDA to identify establishments that manufacture, process, pack, or hold food, drugs, medical devices, or other FDA-regulated products. Weleda AG's FEI number is 1000326682.

What types of violations has Weleda AG received?

Weleda AG has been cited for 9 different violation type(s). Common FDA violations include adulteration (unsafe or unsanitary products), misbranding (incorrect or misleading labels), and regulatory non-compliance.

Where does this information about Weleda AG come from?

All FDA import refusal data for Weleda AG is sourced from the official FDA Data Dashboard (datadashboard.fda.gov), a public government database maintained by the U.S. Food and Drug Administration.

Data sourced from the FDA Data Dashboard, a public database maintained by the U.S. Food and Drug Administration.