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HAAL IZA

⚠️ High Risk

FEI: 3013972344 • Istanbul • TURKEY

FEI

FEI Number

3013972344

📍

Location

Istanbul

🇹🇷

Country

TURKEY
🏢

Address

Nakkasyolu No 10, , Istanbul, , Turkey

High Risk

FDA Import Risk Assessment

62.8
LowModerateHighCritical

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

Statistics

32
Total Refusals
7
Unique Violations
2/9/2023
Latest Refusal
2/14/2018
Earliest Refusal

Score Breakdown

Violation Severity
78.0×40%
Refusal Volume
56.2×30%
Recency
41.6×20%
Frequency
64.1×10%
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

7532×

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).

7128×

NO LICENSE

The article is subject to refusal of admission under section 801(a)(3) of the Federal Food, Drug, and Cosmetic Act (FD&C Act) because it appears to be a biological product for which a biologics license is not in effect under the Public Health Service Act, Part F, Subpart 1-Biological Products, Section 351(a), and it is not the subject of an Investigational New Drug application that is in effect. Therefore, it appears to be a new drug under 201(p) of the FD&C Act that it is in violation of section 505(a) of the FD&C Act because it lacks a new drug approval and because it is misbranded under section 502(f)(1)of the FD&C Act because it fails to bear adequate directions for use

328011×

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.

11811×

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).

4722×

NO ENGLISH

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

271×

DRUG GMPS

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the methods used in and controls used for the manufacture, processing, packing, or holding of drugs and other products do not appear to conform to current good manufacturing practices within the meaning of Section 501(a)(2)(B).

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.

Refusal History

DateProductViolationsDivision
2/9/2023
65QAY02BOTOX
75UNAPPROVED
Division of Northeast Imports (DNEI)
3/29/2018
65QCP02BOTOX
71NO LICENSE
75UNAPPROVED
Division of Southeast Imports (DSEI)
3/15/2018
65QCP02BOTOX
118NOT LISTED
3280FRNMFGREG
71NO LICENSE
75UNAPPROVED
Division of Southeast Imports (DSEI)
3/15/2018
65QCP02BOTOX
118NOT LISTED
3280FRNMFGREG
71NO LICENSE
75UNAPPROVED
Division of Southeast Imports (DSEI)
3/15/2018
65QCP02BOTOX
118NOT LISTED
3280FRNMFGREG
71NO LICENSE
75UNAPPROVED
Division of Southeast Imports (DSEI)
3/15/2018
65QCP02BOTOX
118NOT LISTED
3280FRNMFGREG
71NO LICENSE
75UNAPPROVED
Division of Southeast Imports (DSEI)
3/15/2018
65QCP02BOTOX
118NOT LISTED
3280FRNMFGREG
71NO LICENSE
75UNAPPROVED
Division of Southeast Imports (DSEI)
3/15/2018
65QCP02BOTOX
118NOT LISTED
3280FRNMFGREG
71NO LICENSE
75UNAPPROVED
Division of Southeast Imports (DSEI)
3/15/2018
65QCP02BOTOX
118NOT LISTED
3280FRNMFGREG
71NO LICENSE
75UNAPPROVED
Division of Southeast Imports (DSEI)
3/15/2018
65QBY02BOTOX
16DIRECTIONS
71NO LICENSE
75UNAPPROVED
Division of Northern Border Imports (DNBI)
3/14/2018
65QCP02BOTOX
118NOT LISTED
3280FRNMFGREG
71NO LICENSE
75UNAPPROVED
Division of Southeast Imports (DSEI)
3/14/2018
65QCP02BOTOX
118NOT LISTED
3280FRNMFGREG
71NO LICENSE
75UNAPPROVED
Division of Southeast Imports (DSEI)
3/14/2018
65QCP02BOTOX
118NOT LISTED
3280FRNMFGREG
71NO LICENSE
75UNAPPROVED
Division of Southeast Imports (DSEI)
3/9/2018
66VCP99MISCELLANEOUS PATENT MEDICINES, ETC.
472NO ENGLISH
75UNAPPROVED
Division of Southeast Imports (DSEI)
3/8/2018
64GCY29LEVONORGESTREL (ESTROGEN)
472NO ENGLISH
75UNAPPROVED
Division of Southeast Imports (DSEI)
3/6/2018
65QCP02BOTOX
71NO LICENSE
75UNAPPROVED
Division of Southeast Imports (DSEI)
3/6/2018
65QCP02BOTOX
71NO LICENSE
75UNAPPROVED
Division of Southeast Imports (DSEI)
3/6/2018
65QCP02BOTOX
71NO LICENSE
75UNAPPROVED
Division of Southeast Imports (DSEI)
3/6/2018
65QCP02BOTOX
71NO LICENSE
75UNAPPROVED
Division of Southeast Imports (DSEI)
3/6/2018
65QCP02BOTOX
71NO LICENSE
75UNAPPROVED
Division of Southeast Imports (DSEI)
3/6/2018
65QCP02BOTOX
71NO LICENSE
75UNAPPROVED
Division of Southeast Imports (DSEI)
3/6/2018
65QCP02BOTOX
71NO LICENSE
75UNAPPROVED
Division of Southeast Imports (DSEI)
3/5/2018
65QCP02BOTOX
71NO LICENSE
75UNAPPROVED
Division of Southeast Imports (DSEI)
3/5/2018
65QCP02BOTOX
71NO LICENSE
75UNAPPROVED
Division of Southeast Imports (DSEI)
3/5/2018
65QCP02BOTOX
71NO LICENSE
75UNAPPROVED
Division of Southeast Imports (DSEI)
3/5/2018
65QCP02BOTOX
71NO LICENSE
75UNAPPROVED
Division of Southeast Imports (DSEI)
3/5/2018
65QCP02BOTOX
71NO LICENSE
75UNAPPROVED
Division of Southeast Imports (DSEI)
3/5/2018
65QCP02BOTOX
71NO LICENSE
75UNAPPROVED
Division of Southeast Imports (DSEI)
2/26/2018
65QCP02BOTOX
118NOT LISTED
3280FRNMFGREG
71NO LICENSE
75UNAPPROVED
Division of Northern Border Imports (DNBI)
2/26/2018
60YCP01AFLIBERCEPT (INHIBITOR (GROWTH FACTOR))
27DRUG GMPS
75UNAPPROVED
Division of Southeast Imports (DSEI)
2/15/2018
65QCP02BOTOX
71NO LICENSE
75UNAPPROVED
Division of Southeast Imports (DSEI)
2/14/2018
65QCP02BOTOX
71NO LICENSE
75UNAPPROVED
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is HAAL IZA's FDA import refusal history?

HAAL IZA (FEI: 3013972344) has 32 FDA import refusal record(s) in our database, spanning from 2/14/2018 to 2/9/2023.

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. HAAL IZA's FEI number is 3013972344.

What types of violations has HAAL IZA received?

HAAL IZA has been cited for 7 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 HAAL IZA come from?

All FDA import refusal data for HAAL IZA 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.