MECRO SYSTEM SRL
⚠️ Moderate Risk
FEI: 3015976678 • Ramnicu Valcea, Valcea • ROMANIA
FEI Number
3015976678
Location
Ramnicu Valcea, Valcea
Country
ROMANIAAddress
Strada Uzinei Nr. 4, , Ramnicu Valcea, Valcea, 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
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.
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.
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.
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)).
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).
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.
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)).
INSANITARY
The article is subject to refusal of admission pursuant to section 801(a)(3) in that the article appears to have been prepared, packed, or held under insanitary conditions whereby it may have been contaminated with filth, or whereby it may have been rendered injurious to health.
STD 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(g)(2) 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 under Section 401 of the FD&C Act and the article is not labeled with the name specified in the definition and standard, or the label does not bear the common names of optional ingredients (other than spices, flavoring and coloring) present in such food, insofar as may be required by such regulation.
DIRSEXMPT
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be a drug within the meaning of Section 201(g) and it lacks adequate directions for use.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 1/28/2020 | 29WGT01BOTTLED WATER | Division of Southeast Imports (DSEI) | |
| 8/5/2019 | 29WHY01BOTTLED WATER | 2280DIRSEXMPT | Division of Southeast Imports (DSEI) |
| 7/30/2019 | 29WGY01BOTTLED WATER | Division of Southeast Imports (DSEI) | |
| 7/23/2019 | 29WHT01BOTTLED WATER | 75UNAPPROVED | Division of Southeast Imports (DSEI) |
| 3/21/2019 | 29WHY01BOTTLED WATER | 260FALSE | Division of Southeast Imports (DSEI) |
| 3/21/2019 | 29WHY01BOTTLED WATER | 260FALSE | Division of Southeast Imports (DSEI) |
| 3/21/2019 | 29WHY01BOTTLED WATER | 260FALSE | Division of Southeast Imports (DSEI) |
| 3/21/2019 | 29WGT01BOTTLED WATER | Division of Southeast Imports (DSEI) | |
| 3/21/2019 | 29WHY01BOTTLED WATER | Division of Southeast Imports (DSEI) | |
| 3/21/2019 | 29WHY01BOTTLED WATER | Division of Southeast Imports (DSEI) | |
| 3/21/2019 | 29WYY01BOTTLED WATER | Division of Southeast Imports (DSEI) | |
| 3/21/2019 | 29WGT01BOTTLED WATER | Division of Southeast Imports (DSEI) | |
| 3/19/2019 | 29WGT01BOTTLED WATER | Division of Southeast Imports (DSEI) | |
| 3/19/2019 | 29WGT01BOTTLED WATER | Division of Southeast Imports (DSEI) | |
| 3/14/2019 | 29WGT01BOTTLED WATER | Division of Southeast Imports (DSEI) | |
| 3/14/2019 | 29WGT01BOTTLED WATER | Division of Southeast Imports (DSEI) | |
| 3/14/2019 | 29WGY01BOTTLED WATER | Division of Southeast Imports (DSEI) | |
| 3/8/2019 | 29WGT01BOTTLED WATER | Division of Southeast Imports (DSEI) | |
| 3/6/2019 | 29WHY01BOTTLED WATER | Division of Southeast Imports (DSEI) | |
| 3/6/2019 | 29WGT01BOTTLED WATER | Division of Southeast Imports (DSEI) | |
| 3/6/2019 | 29WGT01BOTTLED WATER | Division of Southeast Imports (DSEI) | |
| 3/6/2019 | 29WGT01BOTTLED WATER | Division of Southeast Imports (DSEI) | |
| 11/28/2018 | 29WHY01BOTTLED WATER | Division of West Coast Imports (DWCI) | |
| 7/12/2018 | 29WHY01BOTTLED WATER | Division of Southeast Imports (DSEI) |
Frequently Asked Questions
What is MECRO SYSTEM SRL's FDA import refusal history?
MECRO SYSTEM SRL (FEI: 3015976678) has 24 FDA import refusal record(s) in our database, spanning from 7/12/2018 to 1/28/2020.
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 SRL's FEI number is 3015976678.
What types of violations has MECRO SYSTEM SRL received?
MECRO SYSTEM SRL has been cited for 10 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 SRL come from?
All FDA import refusal data for MECRO SYSTEM SRL 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.