Teva Czech Industries s.r.o.
⚠️ Moderate Risk
FEI: 1000282452 • Opava, Moravskoslezsky • CZECH REPUBLIC
FEI Number
1000282452
Location
Opava, Moravskoslezsky
Country
CZECH REPUBLICAddress
Ostravska 305/29, , Opava, Moravskoslezsky, Czech Republic
Moderate Risk
FDA Import Risk Assessment
This firm has a moderate history of FDA import refusals. Some attention may be warranted.
Statistics
Score Breakdown
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
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).
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.
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).
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.
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.
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.
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.
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.
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)).
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).
NO ENGLISH
Required label or labeling appears to not be in English in violation of 21 C.F.R. 801.15(c)(1)
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
| Date | Product | Violations | Division |
|---|---|---|---|
| 9/19/2018 | 61TCS13METOPIMAZINE (ANTI-EMETIC/NAUSEANT) | Division of Northeast Imports (DNEI) | |
| 5/25/2017 | 65VBA99SEDATIVE N.E.C. | 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) | New Orleans District Office (NOL-DO) | |
| 7/5/2013 | 63BCQ25FLUTICASONE PROPIONATE (BRONCHODILATOR) | 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) | 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. | New York District Office (NYK-DO) | |
| 11/9/2009 | 54FYT99HERBALS & BOTANICALS (NOT TEAS), N.E.C. | New York District Office (NYK-DO) | |
| 11/9/2009 | 54FYL99HERBALS & BOTANICALS (NOT TEAS), N.E.C. | 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) | New York District Office (NYK-DO) | |
| 12/18/2006 | 60CDL46NAPHAZOLINE HCL (ADRENERGIC) | New York District Office (NYK-DO) | |
| 9/19/2005 | 65QDE99RELAXANT N.E.C. | 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.