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Labora S.R.O.

⚠️ Moderate Risk

FEI: 3004433773 • Tepla • CZECH REPUBLIC

FEI

FEI Number

3004433773

📍

Location

Tepla

🇨🇿
🏢

Address

Dobra Voda 20, U TOUZIME, Tepla, , Czech Republic

Moderate Risk

FDA Import Risk Assessment

45.6
LowModerateHighCritical

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

Statistics

10
Total Refusals
4
Unique Violations
6/18/2013
Latest Refusal
6/18/2013
Earliest Refusal

Score Breakdown

Violation Severity
60.0×40%
Refusal Volume
38.6×30%
Recency
0.0×20%
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

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).

1610×

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.

374110×

FRNMFGREG

The article is subject to refusal of admission pursuant to section 801(o) in that it is being imported or offered for import into the United States, and the importer, owner, or consignee of such article did not, at the time of offering the article for import, submit to the Secretary a statement that identifies the registration under section 510(i) of the Act of each establishment that with respect to such article is required under such section to register with the Secretary.

7510×

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
6/18/2013
66YCY99EXHIBITS - OTHER DRUG RELATED ITEMS N.E.C.
118NOT LISTED
16DIRECTIONS
3741FRNMFGREG
75UNAPPROVED
Division of Northeast Imports (DNEI)
6/18/2013
66YCY99EXHIBITS - OTHER DRUG RELATED ITEMS N.E.C.
118NOT LISTED
16DIRECTIONS
3741FRNMFGREG
75UNAPPROVED
Division of Northeast Imports (DNEI)
6/18/2013
66YCY99EXHIBITS - OTHER DRUG RELATED ITEMS N.E.C.
118NOT LISTED
16DIRECTIONS
3741FRNMFGREG
75UNAPPROVED
Division of Northeast Imports (DNEI)
6/18/2013
66YCY99EXHIBITS - OTHER DRUG RELATED ITEMS N.E.C.
118NOT LISTED
16DIRECTIONS
3741FRNMFGREG
75UNAPPROVED
Division of Northeast Imports (DNEI)
6/18/2013
66YCY99EXHIBITS - OTHER DRUG RELATED ITEMS N.E.C.
118NOT LISTED
16DIRECTIONS
3741FRNMFGREG
75UNAPPROVED
Division of Northeast Imports (DNEI)
6/18/2013
66YCY99EXHIBITS - OTHER DRUG RELATED ITEMS N.E.C.
118NOT LISTED
16DIRECTIONS
3741FRNMFGREG
75UNAPPROVED
Division of Northeast Imports (DNEI)
6/18/2013
66YCY99EXHIBITS - OTHER DRUG RELATED ITEMS N.E.C.
118NOT LISTED
16DIRECTIONS
3741FRNMFGREG
75UNAPPROVED
Division of Northeast Imports (DNEI)
6/18/2013
66YCY99EXHIBITS - OTHER DRUG RELATED ITEMS N.E.C.
118NOT LISTED
16DIRECTIONS
3741FRNMFGREG
75UNAPPROVED
Division of Northeast Imports (DNEI)
6/18/2013
66YCY99EXHIBITS - OTHER DRUG RELATED ITEMS N.E.C.
118NOT LISTED
16DIRECTIONS
3741FRNMFGREG
75UNAPPROVED
Division of Northeast Imports (DNEI)
6/18/2013
66YCY99EXHIBITS - OTHER DRUG RELATED ITEMS N.E.C.
118NOT LISTED
16DIRECTIONS
3741FRNMFGREG
75UNAPPROVED
Division of Northeast Imports (DNEI)

Frequently Asked Questions

What is Labora S.R.O.'s FDA import refusal history?

Labora S.R.O. (FEI: 3004433773) has 10 FDA import refusal record(s) in our database, spanning from 6/18/2013 to 6/18/2013.

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. Labora S.R.O.'s FEI number is 3004433773.

What types of violations has Labora S.R.O. received?

Labora S.R.O. has been cited for 4 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 Labora S.R.O. come from?

All FDA import refusal data for Labora 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.