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AUTONOMOS AB (STROFALIS)

✅ Low Risk

FEI: 3013186782 • Athens • GREECE

FEI

FEI Number

3013186782

📍

Location

Athens

🇬🇷

Country

GREECE
🏢

Address

12131 Peristeri, Gennadiou 1-5, Athens, , Greece

Low Risk

FDA Import Risk Assessment

18.3
LowModerateHighCritical

This firm has a minimal history of FDA import refusals with low-severity violations.

Statistics

1
Total Refusals
2
Unique Violations
9/8/2017
Latest Refusal
9/8/2017
Earliest Refusal

Score Breakdown

Violation Severity
35.0×40%
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

3201×

LACKS FIRM

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(e)(1) of the FD&C Act in that the food is in package form and the label fails to bear the name and place of business of the manufacturer, packer, or distributor.

4731×

LABELING

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

Refusal History

DateProductViolationsDivision
9/8/2017
54ABA13VITAMIN C (ASCORBIC ACID)
320LACKS FIRM
473LABELING
Division of Northeast Imports (DNEI)

Frequently Asked Questions

What is AUTONOMOS AB (STROFALIS)'s FDA import refusal history?

AUTONOMOS AB (STROFALIS) (FEI: 3013186782) has 1 FDA import refusal record(s) in our database, spanning from 9/8/2017 to 9/8/2017.

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. AUTONOMOS AB (STROFALIS)'s FEI number is 3013186782.

What types of violations has AUTONOMOS AB (STROFALIS) received?

AUTONOMOS AB (STROFALIS) has been cited for 2 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 AUTONOMOS AB (STROFALIS) come from?

All FDA import refusal data for AUTONOMOS AB (STROFALIS) 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.