ImportRefusal LogoImportRefusal

Biotika a.s.

⚠️ Moderate Risk

FEI: 3003370212 • Slovenska Lupca, Banska Bystrica • SLOVAKIA

FEI

FEI Number

3003370212

📍

Location

Slovenska Lupca, Banska Bystrica

🇸🇰

Country

SLOVAKIA
🏢

Address

Slovenska Lupca 566, , Slovenska Lupca, Banska Bystrica, Slovakia

Moderate Risk

FDA Import Risk Assessment

27.1
LowModerateHighCritical

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

Statistics

2
Total Refusals
4
Unique Violations
8/22/2006
Latest Refusal
7/22/2005
Earliest Refusal

Score Breakdown

Violation Severity
50.0×40%
Refusal Volume
17.7×30%
Recency
0.0×20%
Frequency
18.4×10%
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).

161×

DIRECTIONS

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it is a device whose label appears to not bear adequate directions for use.

28801×

RXCOMPOUND

the labeling fails to bear, at a minimum, the symbol "Rx only."

3361×

INCONSPICU

Information required by the Act to be on the label or labeling does not appear to be conspicuous enough as to render it likely to be read and understood by the ordinary individual under customary conditions of purchase and use.

Refusal History

DateProductViolationsDivision
8/22/2006
65HCR02DEXTRAN 70 (PLASMA VOLUME EXTENDER)
16DIRECTIONS
2880RXCOMPOUND
336INCONSPICU
Detroit District Office (DET-DO)
7/22/2005
65HAZ02DEXTRAN 70 (PLASMA VOLUME EXTENDER)
118NOT LISTED
New York District Office (NYK-DO)

Frequently Asked Questions

What is Biotika a.s.'s FDA import refusal history?

Biotika a.s. (FEI: 3003370212) has 2 FDA import refusal record(s) in our database, spanning from 7/22/2005 to 8/22/2006.

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. Biotika a.s.'s FEI number is 3003370212.

What types of violations has Biotika a.s. received?

Biotika a.s. has been cited for 4 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 Biotika a.s. come from?

All FDA import refusal data for Biotika a.s. 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.