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SC SCANDIA ROMANA SA SIBIU

⚠️ Moderate Risk

FEI: 3007015892 • Sibiu, Sibiu • ROMANIA

FEI

FEI Number

3007015892

📍

Location

Sibiu, Sibiu

🇷🇴

Country

ROMANIA
🏢

Address

Strada Morilor Nr 45, , Sibiu, Sibiu, Romania

Moderate Risk

FDA Import Risk Assessment

40.1
LowModerateHighCritical

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

Statistics

12
Total Refusals
5
Unique Violations
9/21/2010
Latest Refusal
10/21/2008
Earliest Refusal

Score Breakdown

Violation Severity
53.6×40%
Refusal Volume
41.3×30%
Recency
0.0×20%
Frequency
62.6×10%
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

25612×

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)).

8312×

NO PROCESS

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the manufacturer's failure to file a scheduled process demonstrates that the product is not being manufactured under the mandatory provisions of 21 CFR Part 108 and therefore appears to have been manufactured, processed, or packed, under insanitary conditions whereby it may have been rendered injurious to health.

4829×

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.

2187×

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.

627×

NEEDS FCE

It appears the manufacturer is not registered as a low acid canned food or acidified food manufacturer pursuant to 21 CFR 108.25(c)(1) or 108.35(c)(1).

Refusal History

DateProductViolationsDivision
9/21/2010
25FEE99MIXED VEGETABLES, DRIED OR PASTE, N.E.C.
256INCONSPICU
482NUTRIT LBL
62NEEDS FCE
83NO PROCESS
Detroit District Office (DET-DO)
9/21/2010
25FEE99MIXED VEGETABLES, DRIED OR PASTE, N.E.C.
256INCONSPICU
482NUTRIT LBL
62NEEDS FCE
83NO PROCESS
Detroit District Office (DET-DO)
9/21/2010
25FEE99MIXED VEGETABLES, DRIED OR PASTE, N.E.C.
256INCONSPICU
482NUTRIT LBL
62NEEDS FCE
83NO PROCESS
Detroit District Office (DET-DO)
9/21/2010
25FEE99MIXED VEGETABLES, DRIED OR PASTE, N.E.C.
256INCONSPICU
482NUTRIT LBL
62NEEDS FCE
83NO PROCESS
Detroit District Office (DET-DO)
12/16/2009
18YEI99VEGETABLE PROTEIN PRODUCTS NOT ELSEWHERE MENTIONED, N.E.C.
218LIST INGRE
256INCONSPICU
62NEEDS FCE
83NO PROCESS
Detroit District Office (DET-DO)
12/16/2009
18YEI99VEGETABLE PROTEIN PRODUCTS NOT ELSEWHERE MENTIONED, N.E.C.
218LIST INGRE
256INCONSPICU
62NEEDS FCE
83NO PROCESS
Detroit District Office (DET-DO)
12/16/2009
25YEE99VEGETABLE & VEGETABLE PRODUCTS NOT MENTIONED ELSEWHERE, N.E.C.
218LIST INGRE
256INCONSPICU
62NEEDS FCE
83NO PROCESS
Detroit District Office (DET-DO)
10/21/2008
25FEE99MIXED VEGETABLES, DRIED OR PASTE, N.E.C.
256INCONSPICU
482NUTRIT LBL
83NO PROCESS
Detroit District Office (DET-DO)
10/21/2008
25FEE99MIXED VEGETABLES, DRIED OR PASTE, N.E.C.
218LIST INGRE
256INCONSPICU
482NUTRIT LBL
83NO PROCESS
Detroit District Office (DET-DO)
10/21/2008
25FEE99MIXED VEGETABLES, DRIED OR PASTE, N.E.C.
218LIST INGRE
256INCONSPICU
482NUTRIT LBL
83NO PROCESS
Detroit District Office (DET-DO)
10/21/2008
25FEE99MIXED VEGETABLES, DRIED OR PASTE, N.E.C.
218LIST INGRE
256INCONSPICU
482NUTRIT LBL
83NO PROCESS
Detroit District Office (DET-DO)
10/21/2008
25FEE99MIXED VEGETABLES, DRIED OR PASTE, N.E.C.
218LIST INGRE
256INCONSPICU
482NUTRIT LBL
83NO PROCESS
Detroit District Office (DET-DO)

Frequently Asked Questions

What is SC SCANDIA ROMANA SA SIBIU's FDA import refusal history?

SC SCANDIA ROMANA SA SIBIU (FEI: 3007015892) has 12 FDA import refusal record(s) in our database, spanning from 10/21/2008 to 9/21/2010.

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. SC SCANDIA ROMANA SA SIBIU's FEI number is 3007015892.

What types of violations has SC SCANDIA ROMANA SA SIBIU received?

SC SCANDIA ROMANA SA SIBIU has been cited for 5 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 SC SCANDIA ROMANA SA SIBIU come from?

All FDA import refusal data for SC SCANDIA ROMANA SA SIBIU 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.