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San Miguel Corp

⚠️ Moderate Risk

FEI: 3001757836 • Pasig Mtero Manila • PHILIPPINES

FEI

FEI Number

3001757836

📍

Location

Pasig Mtero Manila

🇵🇭
🏢

Address

Emerald St, , Pasig Mtero Manila, , Philippines

Moderate Risk

FDA Import Risk Assessment

31.4
LowModerateHighCritical

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

Statistics

5
Total Refusals
6
Unique Violations
8/4/2008
Latest Refusal
8/4/2008
Earliest Refusal

Score Breakdown

Violation Severity
44.3×40%
Refusal Volume
28.8×30%
Recency
0.0×20%
Frequency
50.0×10%
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

3215×

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.

4823×

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.

643×

YELLOW #5

The food appears to bear or contain the color additive FD & C Yellow No. 5, which is not declared on the label per 21 CFR 74.705(a)(c) under section 721.

111×

UNSAFE COL

The article appears to be, or to bear or contain a color additive which is unsafe within the meaning of Section 721(a).

2181×

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.

2741×

COLOR LBLG

The article appears to contain an artificial coloring and it fails to bear labeling stating that fact.

Refusal History

DateProductViolationsDivision
8/4/2008
30JDT02BEVERAGE BASE, IMITATION CITRUS
321LACKS N/C
482NUTRIT LBL
Los Angeles District Office (LOS-DO)
8/4/2008
30JDT06BEVERAGE BASE, IMITATION SUBTROPICAL OR TROPICAL FRUIT
321LACKS N/C
64YELLOW #5
Los Angeles District Office (LOS-DO)
8/4/2008
30JDT04BEVERAGE BASE, IMITATION MIXED FRUIT
274COLOR LBLG
321LACKS N/C
482NUTRIT LBL
64YELLOW #5
Los Angeles District Office (LOS-DO)
8/4/2008
30JDT06BEVERAGE BASE, IMITATION SUBTROPICAL OR TROPICAL FRUIT
218LIST INGRE
321LACKS N/C
482NUTRIT LBL
Los Angeles District Office (LOS-DO)
8/4/2008
30JDT02BEVERAGE BASE, IMITATION CITRUS
11UNSAFE COL
321LACKS N/C
64YELLOW #5
Los Angeles District Office (LOS-DO)

Frequently Asked Questions

What is San Miguel Corp's FDA import refusal history?

San Miguel Corp (FEI: 3001757836) has 5 FDA import refusal record(s) in our database, spanning from 8/4/2008 to 8/4/2008.

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. San Miguel Corp's FEI number is 3001757836.

What types of violations has San Miguel Corp received?

San Miguel Corp has been cited for 6 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 San Miguel Corp come from?

All FDA import refusal data for San Miguel Corp 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.