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Teva Czech Industries s.r.o.

⚠️ Moderate Risk

FEI: 1000282452 • Opava, Moravskoslezsky • CZECH REPUBLIC

FEI

FEI Number

1000282452

📍

Location

Opava, Moravskoslezsky

🇨🇿
🏢

Address

Ostravska 305/29, , Opava, Moravskoslezsky, Czech Republic

Moderate Risk

FDA Import Risk Assessment

39.4
LowModerateHighCritical

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

Statistics

22
Total Refusals
12
Unique Violations
9/19/2018
Latest Refusal
7/30/2003
Earliest Refusal

Score Breakdown

Violation Severity
56.9×40%
Refusal Volume
50.4×30%
Recency
0.0×20%
Frequency
14.5×10%
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

11810×

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).

167×

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.

755×

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).

2183×

LIST INGRE

The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of Section 403(i)(2) of the FD&C Act in that it is fabricated from two or more ingredients and the label fails to bear the common or usual name of each such ingredient and/or the article purports to be a beverage containing vegetable or fruit juice, but does not bear a statement with appropriate prominence on the information panel of the total percentage of such fruit or vegetable juice contained in the food.

32803×

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.

4823×

NUTRIT LBL

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be misbranded in that the label or labeling fails to bear the required nutrition information.

723×

NEW VET DR

The article is subject to refusal of admission pursuant to Section 801(a)(3) of the Federal Food, Drug, and Cosmetic Act in that it appears to be a new animal drug that is unsafe within the meaning of Section 512(a) of the Federal Food, Drug, and Cosmetic Act as it is not the subject of an approved new animal drug application, conditionally approved new animal drug application, or index listing, and no investigational new animal drug exemption applies.

23003×

DIETARYLBL

The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it is a dietary supplement that appears to be misbranded within the meaning of Section 403(s)(2)(B) of the FD&C Act in that the label or labeling fails to identify the product by using the term "dietary supplement", which term may be modified with the name of such an ingredient.

2562×

INCONSPICU

The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of Section 403(f) of the FD&C Act in that any word, statement, or other information required by or under the authority of the FD&C Act to appear on the label or labeling is not prominently placed thereon with such conspicuousness (as compared with other words, statements, designs, or devices, in the labeling) and in such terms as to render it likely to be read and understood by the ordinary individual under customary terms of purchase and use (for example, label contains information in two or more languages but fails to repeat all required information in both languages in accordance with 21 CFR 101.15(c)(2), or label fails to include all required information in English in accordance with 21 CFR 101.15(c)(1), except in the case of articles distributed solely in the Commonwealth of Puerto Rico or in a Territory where the predominant language is one other than English)).

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).

32601×

NO ENGLISH

Required label or labeling appears to not be in English in violation of 21 C.F.R. 801.15(c)(1)

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
9/19/2018
61TCS13METOPIMAZINE (ANTI-EMETIC/NAUSEANT)
118NOT LISTED
16DIRECTIONS
Division of Northeast Imports (DNEI)
5/25/2017
65VBA99SEDATIVE N.E.C.
118NOT LISTED
16DIRECTIONS
3280FRNMFGREG
472NO ENGLISH
Division of Northeast Imports (DNEI)
3/13/2014
61XCI49AZELASTINE, ANTI-HISTAMINE (ANTI-HISTAMINIC)
75UNAPPROVED
New Orleans District Office (NOL-DO)
7/31/2013
62ICS99ANTI-NEOPLASTIC N.E.C.
16DIRECTIONS
Philadelphia District Office (PHI-DO)
7/5/2013
63BCQ25FLUTICASONE PROPIONATE (BRONCHODILATOR)
118NOT LISTED
3280FRNMFGREG
75UNAPPROVED
New Orleans District Office (NOL-DO)
7/5/2013
63BCQ25FLUTICASONE PROPIONATE (BRONCHODILATOR)
118NOT LISTED
3280FRNMFGREG
75UNAPPROVED
New Orleans District Office (NOL-DO)
3/30/2012
62JCS14PERGOLIDE MESYLATE (ANTI-PARKINSONIAN)
72NEW VET DR
Southwest Import District Office (SWI-DO)
3/30/2012
62JCS14PERGOLIDE MESYLATE (ANTI-PARKINSONIAN)
72NEW VET DR
Southwest Import District Office (SWI-DO)
6/7/2011
64FCR24BROMOCRIPTINE MESYLATE (ENZYME INHIBITOR)
118NOT LISTED
27DRUG GMPS
New York District Office (NYK-DO)
9/16/2010
54YYY99VITAMIN, MINERAL, PROTEINS AND UNCONVENTIONAL DIETARY SPECIALITIES FOR HUMANS AND ANIMALS, N.E.C.
3260NO ENGLISH
New York District Office (NYK-DO)
2/1/2010
62JAS14PERGOLIDE MESYLATE (ANTI-PARKINSONIAN)
72NEW VET DR
Los Angeles District Office (LOS-DO)
11/9/2009
54FYL99HERBALS & BOTANICALS (NOT TEAS), N.E.C.
218LIST INGRE
2300DIETARYLBL
482NUTRIT LBL
New York District Office (NYK-DO)
11/9/2009
54FYT99HERBALS & BOTANICALS (NOT TEAS), N.E.C.
218LIST INGRE
2300DIETARYLBL
256INCONSPICU
482NUTRIT LBL
New York District Office (NYK-DO)
11/9/2009
54FYL99HERBALS & BOTANICALS (NOT TEAS), N.E.C.
218LIST INGRE
2300DIETARYLBL
256INCONSPICU
482NUTRIT LBL
New York District Office (NYK-DO)
9/1/2009
54FYL99HERBALS & BOTANICALS (NOT TEAS), N.E.C.
16DIRECTIONS
New York District Office (NYK-DO)
7/21/2009
54FYL99HERBALS & BOTANICALS (NOT TEAS), N.E.C.
118NOT LISTED
New York District Office (NYK-DO)
7/21/2009
54FYL99HERBALS & BOTANICALS (NOT TEAS), N.E.C.
118NOT LISTED
New York District Office (NYK-DO)
6/5/2009
64HBL02GUAIFENESIN (EXPECTORANT)
118NOT LISTED
16DIRECTIONS
New York District Office (NYK-DO)
12/18/2006
60CDL46NAPHAZOLINE HCL (ADRENERGIC)
118NOT LISTED
75UNAPPROVED
New York District Office (NYK-DO)
9/19/2005
65QDE99RELAXANT N.E.C.
118NOT LISTED
75UNAPPROVED
New York District Office (NYK-DO)
1/21/2004
62JMS14PERGOLIDE MESYLATE (ANTI-PARKINSONIAN)
16DIRECTIONS
New York District Office (NYK-DO)
7/30/2003
62JSY14PERGOLIDE MESYLATE (ANTI-PARKINSONIAN)
16DIRECTIONS
Cincinnati District Office (CIN-DO)

Frequently Asked Questions

What is Teva Czech Industries s.r.o.'s FDA import refusal history?

Teva Czech Industries s.r.o. (FEI: 1000282452) has 22 FDA import refusal record(s) in our database, spanning from 7/30/2003 to 9/19/2018.

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. Teva Czech Industries s.r.o.'s FEI number is 1000282452.

What types of violations has Teva Czech Industries s.r.o. received?

Teva Czech Industries s.r.o. has been cited for 12 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 Teva Czech Industries s.r.o. come from?

All FDA import refusal data for Teva Czech Industries s.r.o. 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.