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PK BAS

⚠️ Moderate Risk

FEI: 3013545498 • Schenefeld, Schleswig-Holstein • GERMANY

FEI

FEI Number

3013545498

📍

Location

Schenefeld, Schleswig-Holstein

🇩🇪

Country

GERMANY
🏢

Address

Industriestr. 2D, , Schenefeld, Schleswig-Holstein, Germany

Moderate Risk

FDA Import Risk Assessment

25.7
LowModerateHighCritical

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

Statistics

3
Total Refusals
1
Unique Violations
7/13/2017
Latest Refusal
7/3/2017
Earliest Refusal

Score Breakdown

Violation Severity
40.0×40%
Refusal Volume
22.3×30%
Recency
0.0×20%
Frequency
30.0×10%
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

4733×

LABELING

The article appears in violation of FPLA because of its placement, form and/or contents statement.

Refusal History

DateProductViolationsDivision
7/13/2017
40PFH99OTHER FORMULA PRODUCTS, N.E.C., POWDER FORMULA
473LABELING
Division of Northern Border Imports (DNBI)
7/3/2017
40PHT01MILK BASE INFANT FORMULA PRODUCT (0-12 MONTHS), POWDER FORMULA
473LABELING
Division of Northern Border Imports (DNBI)
7/3/2017
40PHT01MILK BASE INFANT FORMULA PRODUCT (0-12 MONTHS), POWDER FORMULA
473LABELING
Division of Northern Border Imports (DNBI)

Frequently Asked Questions

What is PK BAS's FDA import refusal history?

PK BAS (FEI: 3013545498) has 3 FDA import refusal record(s) in our database, spanning from 7/3/2017 to 7/13/2017.

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. PK BAS's FEI number is 3013545498.

What types of violations has PK BAS received?

PK BAS has been cited for 1 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 PK BAS come from?

All FDA import refusal data for PK BAS 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.