ImportRefusal LogoImportRefusal

Circassia AB

✅ Low Risk

FEI: 3008662397 • Uppsala, Uppsala Lan • SWEDEN

FEI

FEI Number

3008662397

📍

Location

Uppsala, Uppsala Lan

🇸🇪

Country

SWEDEN
🏢

Address

Hansellisgatan 13, , Uppsala, Uppsala 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
2
Unique Violations
11/12/2002
Latest Refusal
11/12/2002
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

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
11/12/2002
73CCIANALYZER, GAS, NITROGEN, GASEOUS-PHASE
341REGISTERED
508NO 510(K)
Baltimore District Office (BLT-DO)

Frequently Asked Questions

What is Circassia AB's FDA import refusal history?

Circassia AB (FEI: 3008662397) has 1 FDA import refusal record(s) in our database, spanning from 11/12/2002 to 11/12/2002.

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. Circassia AB's FEI number is 3008662397.

What types of violations has Circassia AB received?

Circassia AB 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 Circassia AB come from?

All FDA import refusal data for Circassia 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.