ImportRefusal LogoImportRefusal

BRITISH VITATECH

⚠️ High Risk

FEI: 3038261754 • Leicester, LEC • UNITED KINGDOM

FEI

FEI Number

3038261754

📍

Location

Leicester, LEC

🇬🇧
🏢

Address

1 Brook Street, , Leicester, LEC, United Kingdom

High Risk

FDA Import Risk Assessment

65.9
LowModerateHighCritical

This firm has a significant history of FDA import refusals with notable violations.

Statistics

23
Total Refusals
5
Unique Violations
7/28/2025
Latest Refusal
7/28/2025
Earliest Refusal

Score Breakdown

Violation Severity
56.0×40%
Refusal Volume
51.1×30%
Recency
90.9×20%
Frequency
100.0×10%
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

11823×

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).

328023×

FRNMFGREG

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to be misbranded as defined in section 502(o) of the FD&C Act. It appears that it was manufactured, prepared, propagated, compounded, or processed in an establishment not duly registered under section 510 of the Act.

33623×

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.

48323×

DRUG NAME

The article appears to be a drug and fails to bear the proprietary or established name and/or name and quantity of each active ingredient.

7523×

UNAPPROVED

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be a new drug within the meaning of Section 201(p) without an approved New Drug Application (NDA).

Refusal History

DateProductViolationsDivision
7/28/2025
66BIY05CAFFEINE (STIMULANT)
118NOT LISTED
3280FRNMFGREG
336INCONSPICU
483DRUG NAME
75UNAPPROVED
Division of Southeast Imports (DSEI)
7/28/2025
66BIY05CAFFEINE (STIMULANT)
118NOT LISTED
3280FRNMFGREG
336INCONSPICU
483DRUG NAME
75UNAPPROVED
Division of Southeast Imports (DSEI)
7/28/2025
66BIY05CAFFEINE (STIMULANT)
118NOT LISTED
3280FRNMFGREG
336INCONSPICU
483DRUG NAME
75UNAPPROVED
Division of Southeast Imports (DSEI)
7/28/2025
66BIY05CAFFEINE (STIMULANT)
118NOT LISTED
3280FRNMFGREG
336INCONSPICU
483DRUG NAME
75UNAPPROVED
Division of Southeast Imports (DSEI)
7/28/2025
66BIY05CAFFEINE (STIMULANT)
118NOT LISTED
3280FRNMFGREG
336INCONSPICU
483DRUG NAME
75UNAPPROVED
Division of Southeast Imports (DSEI)
7/28/2025
66BIY05CAFFEINE (STIMULANT)
118NOT LISTED
3280FRNMFGREG
336INCONSPICU
483DRUG NAME
75UNAPPROVED
Division of Southeast Imports (DSEI)
7/28/2025
66BIY05CAFFEINE (STIMULANT)
118NOT LISTED
3280FRNMFGREG
336INCONSPICU
483DRUG NAME
75UNAPPROVED
Division of Southeast Imports (DSEI)
7/28/2025
66BIY05CAFFEINE (STIMULANT)
118NOT LISTED
3280FRNMFGREG
336INCONSPICU
483DRUG NAME
75UNAPPROVED
Division of Southeast Imports (DSEI)
7/28/2025
66BIY05CAFFEINE (STIMULANT)
118NOT LISTED
3280FRNMFGREG
336INCONSPICU
483DRUG NAME
75UNAPPROVED
Division of Southeast Imports (DSEI)
7/28/2025
66BIY05CAFFEINE (STIMULANT)
118NOT LISTED
3280FRNMFGREG
336INCONSPICU
483DRUG NAME
75UNAPPROVED
Division of Southeast Imports (DSEI)
7/28/2025
66BIY05CAFFEINE (STIMULANT)
118NOT LISTED
3280FRNMFGREG
336INCONSPICU
483DRUG NAME
75UNAPPROVED
Division of Southeast Imports (DSEI)
7/28/2025
66BIY05CAFFEINE (STIMULANT)
118NOT LISTED
3280FRNMFGREG
336INCONSPICU
483DRUG NAME
75UNAPPROVED
Division of Southeast Imports (DSEI)
7/28/2025
66BIY05CAFFEINE (STIMULANT)
118NOT LISTED
3280FRNMFGREG
336INCONSPICU
483DRUG NAME
75UNAPPROVED
Division of Southeast Imports (DSEI)
7/28/2025
66BIY05CAFFEINE (STIMULANT)
118NOT LISTED
3280FRNMFGREG
336INCONSPICU
483DRUG NAME
75UNAPPROVED
Division of Southeast Imports (DSEI)
7/28/2025
66BIY05CAFFEINE (STIMULANT)
118NOT LISTED
3280FRNMFGREG
336INCONSPICU
483DRUG NAME
75UNAPPROVED
Division of Southeast Imports (DSEI)
7/28/2025
66BIY05CAFFEINE (STIMULANT)
118NOT LISTED
3280FRNMFGREG
336INCONSPICU
483DRUG NAME
75UNAPPROVED
Division of Southeast Imports (DSEI)
7/28/2025
66BIY05CAFFEINE (STIMULANT)
118NOT LISTED
3280FRNMFGREG
336INCONSPICU
483DRUG NAME
75UNAPPROVED
Division of Southeast Imports (DSEI)
7/28/2025
66BIY05CAFFEINE (STIMULANT)
118NOT LISTED
3280FRNMFGREG
336INCONSPICU
483DRUG NAME
75UNAPPROVED
Division of Southeast Imports (DSEI)
7/28/2025
66BIY05CAFFEINE (STIMULANT)
118NOT LISTED
3280FRNMFGREG
336INCONSPICU
483DRUG NAME
75UNAPPROVED
Division of Southeast Imports (DSEI)
7/28/2025
66BIY05CAFFEINE (STIMULANT)
118NOT LISTED
3280FRNMFGREG
336INCONSPICU
483DRUG NAME
75UNAPPROVED
Division of Southeast Imports (DSEI)
7/28/2025
66BIY05CAFFEINE (STIMULANT)
118NOT LISTED
3280FRNMFGREG
336INCONSPICU
483DRUG NAME
75UNAPPROVED
Division of Southeast Imports (DSEI)
7/28/2025
66BIY05CAFFEINE (STIMULANT)
118NOT LISTED
3280FRNMFGREG
336INCONSPICU
483DRUG NAME
75UNAPPROVED
Division of Southeast Imports (DSEI)
7/28/2025
66BIY05CAFFEINE (STIMULANT)
118NOT LISTED
3280FRNMFGREG
336INCONSPICU
483DRUG NAME
75UNAPPROVED
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is BRITISH VITATECH's FDA import refusal history?

BRITISH VITATECH (FEI: 3038261754) has 23 FDA import refusal record(s) in our database, spanning from 7/28/2025 to 7/28/2025.

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. BRITISH VITATECH's FEI number is 3038261754.

What types of violations has BRITISH VITATECH received?

BRITISH VITATECH has been cited for 5 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 BRITISH VITATECH come from?

All FDA import refusal data for BRITISH VITATECH 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.