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Akla Ab

✅ Low Risk

FEI: 3012071495 • Taby, Stockholms Lan • SWEDEN

FEI

FEI Number

3012071495

📍

Location

Taby, Stockholms Lan

🇸🇪

Country

SWEDEN
🏢

Address

Enhagsslingan 2, , Taby, Stockholms Lan, Sweden

Low Risk

FDA Import Risk Assessment

24.3
LowModerateHighCritical

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

Statistics

1
Total Refusals
3
Unique Violations
2/29/2016
Latest Refusal
2/29/2016
Earliest Refusal

Score Breakdown

Violation Severity
50.0×40%
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

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).

3411×

REGISTERED

It appears the device is subject to listing under 510(j) and the initial distributor has not registered as required by 21 CFR 807.20 (a)(5).

5081×

NO 510(K)

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it is a post 1976 device for which a Section 510(k)application does not appear to have been determined substantially equivalent or otherwise filed.

Refusal History

DateProductViolationsDivision
2/29/2016
79OHOFIRST AID KIT WITHOUT DRUG
118NOT LISTED
341REGISTERED
508NO 510(K)
Philadelphia District Office (PHI-DO)

Frequently Asked Questions

What is Akla Ab's FDA import refusal history?

Akla Ab (FEI: 3012071495) has 1 FDA import refusal record(s) in our database, spanning from 2/29/2016 to 2/29/2016.

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. Akla Ab's FEI number is 3012071495.

What types of violations has Akla Ab received?

Akla Ab has been cited for 3 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 Akla Ab come from?

All FDA import refusal data for Akla Ab 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.