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Fitopharm

✅ Low Risk

FEI: 3004530527 • Novgorodskaya • RUSSIA

FEI

FEI Number

3004530527

📍

Location

Novgorodskaya

🇷🇺

Country

RUSSIA
🏢

Address

Kashenko St 9, , Novgorodskaya, , Russia

Low Risk

FDA Import Risk Assessment

23.0
LowModerateHighCritical

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

Statistics

1
Total Refusals
3
Unique Violations
1/26/2010
Latest Refusal
1/26/2010
Earliest Refusal

Score Breakdown

Violation Severity
46.7×40%
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

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.

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.

4721×

NO ENGLISH

Required label or labeling appears to not be in English in violation of 21 C.F.R. 201.15(c)(1).

Refusal History

DateProductViolationsDivision
1/26/2010
55QG13SYRUP (PHARMACEUTIC NECESSITY - FLAVOR)
16DIRECTIONS
336INCONSPICU
472NO ENGLISH
New York District Office (NYK-DO)

Frequently Asked Questions

What is Fitopharm's FDA import refusal history?

Fitopharm (FEI: 3004530527) has 1 FDA import refusal record(s) in our database, spanning from 1/26/2010 to 1/26/2010.

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. Fitopharm's FEI number is 3004530527.

What types of violations has Fitopharm received?

Fitopharm 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 Fitopharm come from?

All FDA import refusal data for Fitopharm 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.