Gloria SA
⚠️ Moderate Risk
FEI: 3009951042 • Lima, Lima • PERU
FEI Number
3009951042
Location
Lima, Lima
Country
PERUAddress
Lurigancho-Chosica, La Capitana Avenue 190, Lima, Lima, Peru
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
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.
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).
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.
COLOR LBLG
The article appears to contain an artificial coloring and it fails to bear labeling stating that fact.
LABELING
The article appears in violation of FPLA because of its placement, form and/or contents statement.
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.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 9/18/2019 | 09CET03MILK, CONCENTRATED, EVAPORATED AND CONDENSED | 253STD IDENT | Division of West Coast Imports (DWCI) |
| 9/18/2019 | 09DEN03MILK, CONCENTRATED, EVAPORATED, CONDENSED, LOW FAT | 253STD IDENT | Division of West Coast Imports (DWCI) |
| 8/21/2019 | 09CEE03MILK, CONCENTRATED, EVAPORATED AND CONDENSED | 253STD IDENT | Division of Southeast Imports (DSEI) |
| 8/21/2019 | 09CEE03MILK, CONCENTRATED, EVAPORATED AND CONDENSED | 253STD IDENT | Division of Southeast Imports (DSEI) |
| 8/7/2019 | 14AEE07FILLED MILK, CONCENTRATED, EVAPORATED MILK TYPE PRODUCT | 253STD IDENT | Division of Northeast Imports (DNEI) |
| 8/7/2019 | 14AEE07FILLED MILK, CONCENTRATED, EVAPORATED MILK TYPE PRODUCT | 253STD IDENT | Division of Northeast Imports (DNEI) |
| 8/6/2019 | 09CET09MILK, PLAIN | 473LABELING | Division of Southeast Imports (DSEI) |
| 8/6/2019 | 09CET09MILK, PLAIN | 473LABELING | Division of Southeast Imports (DSEI) |
| 12/19/2013 | 24DCP60CORN, JUICE OR DRINK | Los Angeles District Office (LOS-DO) | |
| 6/18/2013 | 24DCP60CORN, JUICE OR DRINK | Los Angeles District Office (LOS-DO) | |
| 1/9/2013 | 24DDF60CORN, JUICE OR DRINK | New York District Office (NYK-DO) |
Frequently Asked Questions
What is Gloria SA's FDA import refusal history?
Gloria SA (FEI: 3009951042) has 11 FDA import refusal record(s) in our database, spanning from 1/9/2013 to 9/18/2019.
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. Gloria SA's FEI number is 3009951042.
What types of violations has Gloria SA received?
Gloria SA 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 Gloria SA come from?
All FDA import refusal data for Gloria SA 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.