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Medbest S.A.

⚠️ Moderate Risk

FEI: 3007499620 • Athens, None of the above • GREECE

FEI

FEI Number

3007499620

📍

Location

Athens, None of the above

🇬🇷

Country

GREECE
🏢

Address

282, Kifisias Avenue, Floor 2nd; Halandri, Athens, None of the above, Greece

Moderate Risk

FDA Import Risk Assessment

33.7
LowModerateHighCritical

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

Statistics

3
Total Refusals
4
Unique Violations
1/12/2016
Latest Refusal
1/8/2013
Earliest Refusal

Score Breakdown

Violation Severity
65.0×40%
Refusal Volume
22.3×30%
Recency
0.0×20%
Frequency
10.0×10%
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

622×

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).

832×

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.

3211×

LACKS N/C

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(e)(2) of the FD&C Act in that the food is in package form and the label fails to bear an accurate statement of the quantity of the contents in terms of weight, measure, or numerical count in accordance with Section 403(e)(2) of the FD&C Act.

4821×

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.

Refusal History

DateProductViolationsDivision
1/12/2016
28AYT60PEPPER, MIXED
482NUTRIT LBL
New Orleans District Office (NOL-DO)
1/8/2013
21GCO11OLIVES, GREEN, (PIT FRUIT)
321LACKS N/C
62NEEDS FCE
83NO PROCESS
Seattle District Office (SEA-DO)
1/8/2013
21GCO11OLIVES, GREEN, (PIT FRUIT)
62NEEDS FCE
83NO PROCESS
Seattle District Office (SEA-DO)

Frequently Asked Questions

What is Medbest S.A.'s FDA import refusal history?

Medbest S.A. (FEI: 3007499620) has 3 FDA import refusal record(s) in our database, spanning from 1/8/2013 to 1/12/2016.

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. Medbest S.A.'s FEI number is 3007499620.

What types of violations has Medbest S.A. received?

Medbest S.A. 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 Medbest S.A. come from?

All FDA import refusal data for Medbest S.A. 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.