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Pascoe Pharmazeutische Praparate GmbH

⚠️ Moderate Risk

FEI: 3004283488 • Giesen, Hassia • GERMANY

FEI

FEI Number

3004283488

📍

Location

Giesen, Hassia

🇩🇪

Country

GERMANY
🏢

Address

Schiffenberger Weg 55, , Giesen, Hassia, Germany

Moderate Risk

FDA Import Risk Assessment

27.7
LowModerateHighCritical

This firm has a moderate history of FDA import refusals. Some attention may be warranted.

Statistics

1
Total Refusals
6
Unique Violations
7/10/2019
Latest Refusal
7/10/2019
Earliest Refusal

Score Breakdown

Violation Severity
58.3×40%
Refusal Volume
11.2×30%
Recency
0.0×20%
Frequency
10.0×10%
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

1181×

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).

2601×

FALSE

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(a)(1 ) of the FD&C Act in that the labeling is false or misleading in any particular.

271×

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).

32801×

FRNMFGREG

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to be misbranded as defined in section 502(o) of the FD&C Act. It appears that it was manufactured, prepared, propagated, compounded, or processed in an establishment not duly registered under section 510 of the Act.

4721×

NO ENGLISH

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

751×

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).

Refusal History

DateProductViolationsDivision
7/10/2019
66VBP99MISCELLANEOUS PATENT MEDICINES, ETC.
118NOT LISTED
260FALSE
27DRUG GMPS
3280FRNMFGREG
472NO ENGLISH
75UNAPPROVED
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is Pascoe Pharmazeutische Praparate GmbH's FDA import refusal history?

Pascoe Pharmazeutische Praparate GmbH (FEI: 3004283488) has 1 FDA import refusal record(s) in our database, spanning from 7/10/2019 to 7/10/2019.

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. Pascoe Pharmazeutische Praparate GmbH's FEI number is 3004283488.

What types of violations has Pascoe Pharmazeutische Praparate GmbH received?

Pascoe Pharmazeutische Praparate GmbH has been cited for 6 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 Pascoe Pharmazeutische Praparate GmbH come from?

All FDA import refusal data for Pascoe Pharmazeutische Praparate GmbH 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.