Mecro system
⚠️ Moderate Risk
FEI: 3011324805 • Bucharest, Bucharest • ROMANIA
FEI Number
3011324805
Location
Bucharest, Bucharest
Country
ROMANIAAddress
100p, Sector 6, Timisoara blvd, Bucharest, Bucharest, Romania
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
FALSE
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(a)(1 ) of the FD&C Act in that the labeling is false or misleading in any particular.
INSANITARY
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to have been prepared, packed, or held under insanitary conditions whereby it may have become contaminated with filth, or whereby it may have been rendered injurious to health.
NO ENGLISH
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)).
STD IDENT
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(g)(1) of the FD&C Act in that the article purports to be or is represented as a food for which a definition and standard of identity have been prescribed by regulations as provided by section 401 of the FD&C Act and the article does not conform to such definition and standard.
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.
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.
USUAL NAME
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)(1) of the FD&C Act in that the label fails to bear the common or usual name of the food, if any there be.
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).
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).
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 4/17/2018 | 29WGT01BOTTLED WATER | Division of Southeast Imports (DSEI) | |
| 4/17/2018 | 29WHT99WATER AND ICE, N.E.C. | Division of Southeast Imports (DSEI) | |
| 4/17/2018 | 29WHY01BOTTLED WATER | Division of Southeast Imports (DSEI) | |
| 4/17/2018 | 29WHY01BOTTLED WATER | Division of Southeast Imports (DSEI) | |
| 4/17/2018 | 29WHY01BOTTLED WATER | Division of Southeast Imports (DSEI) | |
| 4/17/2018 | 29WHY01BOTTLED WATER | Division of Southeast Imports (DSEI) | |
| 4/17/2018 | 29WGY01BOTTLED WATER | Division of Southeast Imports (DSEI) | |
| 4/17/2018 | 29WGY01BOTTLED WATER | Division of Southeast Imports (DSEI) | |
| 4/17/2018 | 29WHY01BOTTLED WATER | Division of Southeast Imports (DSEI) | |
| 4/17/2018 | 29WGY01BOTTLED WATER | Division of Southeast Imports (DSEI) | |
| 10/27/2017 | 65FIY99WATER N.E.C. (PHARMACEUTIC AID) | Division of Southeast Imports (DSEI) |
Frequently Asked Questions
What is Mecro system's FDA import refusal history?
Mecro system (FEI: 3011324805) has 11 FDA import refusal record(s) in our database, spanning from 10/27/2017 to 4/17/2018.
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. Mecro system's FEI number is 3011324805.
What types of violations has Mecro system received?
Mecro system has been cited for 9 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 Mecro system come from?
All FDA import refusal data for Mecro system 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.