Laboratorios Combisa S.A. de C.V.
⚠️ High Risk
FEI: 3003922103 • San Marcos City, El Salvador • EL SALVADOR
FEI Number
3003922103
Location
San Marcos City, El Salvador
Country
EL SALVADORAddress
Highway to San Marcos N 428, , San Marcos City, El Salvador, El Salvador
High Risk
FDA Import Risk Assessment
This firm has a significant history of FDA import refusals with notable violations.
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
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.
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.
NOT LISTED
It appears the drug or device is not included in a list required by Section 510(j), or a notice or other information respecting it was not provided as required by section 510(j) or 510(k).
UNSAFE ADD
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to bear or contain an unsafe food additive within the meaning of section 409.
HEALTH C
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 bears an unauthorized nutrient content/health claim.
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.
UNSAFE COL
The article appears to be a color additive for the purposes of coloring only in or on drugs or devices, and 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.
COL ADDED
The article appears to bear or contain, for the purpose of coloring only, a color additive which is unsafe within the meaning of Section 721(a).
OMITTED
The article is subject to refusal of admission pursuant Section 801(a)(3) of the FD&C Act in that it appears that a valuable constituent of the article has been in whole or in part omitted or abstracted from the article.
DIETARYLBL
The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it is a dietary supplement that appears to be misbranded within the meaning of Section 403(s)(2)(B) of the FD&C Act in that the label or labeling fails to identify the product by using the term "dietary supplement", which term may be modified with the name of such an ingredient.
COLOR LBLG
The article appears to contain an artificial coloring and it fails to bear labeling stating that fact.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 11/5/2024 | 54ACL90MULTIPLE VITAMINS (MVI-12 VITAMIN COMBO) (VITAMIN) | 260FALSE | Division of Northeast Imports (DNEI) |
| 5/31/2024 | 54ACL90MULTIPLE VITAMINS (MVI-12 VITAMIN COMBO) (VITAMIN) | Division of Northeast Imports (DNEI) | |
| 8/23/2023 | 54BGL01CALCIUM (MINERAL) | 75UNAPPROVED | Division of Southeast Imports (DSEI) |
| 5/23/2019 | 54ACL90MULTIPLE VITAMINS (MVI-12 VITAMIN COMBO) (VITAMIN) | 482NUTRIT LBL | Division of Southwest Imports (DSWI) |
| 5/23/2019 | 54ACL90MULTIPLE VITAMINS (MVI-12 VITAMIN COMBO) (VITAMIN) | 482NUTRIT LBL | Division of Southwest Imports (DSWI) |
| 1/31/2011 | 54ACY90MULTIPLE VITAMINS (MVI-12 VITAMIN COMBO) (VITAMIN) | Los Angeles District Office (LOS-DO) | |
| 10/18/2010 | 54YYY99VITAMIN, MINERAL, PROTEINS AND UNCONVENTIONAL DIETARY SPECIALITIES FOR HUMANS AND ANIMALS, N.E.C. | 488HEALTH C | Southwest Import District Office (SWI-DO) |
| 10/18/2010 | 54ACY90MULTIPLE VITAMINS (MVI-12 VITAMIN COMBO) (VITAMIN) | Southwest Import District Office (SWI-DO) | |
| 10/15/2010 | 54ACY90MULTIPLE VITAMINS (MVI-12 VITAMIN COMBO) (VITAMIN) | Los Angeles District Office (LOS-DO) | |
| 10/15/2010 | 54ACY90MULTIPLE VITAMINS (MVI-12 VITAMIN COMBO) (VITAMIN) | 238UNSAFE ADD | Los Angeles District Office (LOS-DO) |
| 10/15/2010 | 54ACY90MULTIPLE VITAMINS (MVI-12 VITAMIN COMBO) (VITAMIN) | Los Angeles District Office (LOS-DO) | |
| 5/27/2010 | 61XBL14CYPROHEPTADINE HCL (ANTI-HISTAMINIC) | 75UNAPPROVED | Florida District Office (FLA-DO) |
| 4/2/2010 | 54AYL99VITAMIN, N.E.C. | 75UNAPPROVED | Southwest Import District Office (SWI-DO) |
| 9/9/2009 | 60LBJ07CAMPHORATED OIL | 118NOT LISTED | Southwest Import District Office (SWI-DO) |
| 2/6/2009 | 54YCL99VITAMIN, MINERAL, PROTEINS AND UNCONVENTIONAL DIETARY SPECIALITIES FOR HUMANS AND ANIMALS, N.E.C. | 488HEALTH C | Florida District Office (FLA-DO) |
| 1/7/2008 | 54ABH03VITAMIN B2 (RIBOFLAVIN) | 75UNAPPROVED | New York District Office (NYK-DO) |
| 8/29/2007 | 54YGT99VITAMIN, MINERAL, PROTEINS AND UNCONVENTIONAL DIETARY SPECIALITIES FOR HUMANS AND ANIMALS, N.E.C. | 75UNAPPROVED | Baltimore District Office (BLT-DO) |
Frequently Asked Questions
What is Laboratorios Combisa S.A. de C.V.'s FDA import refusal history?
Laboratorios Combisa S.A. de C.V. (FEI: 3003922103) has 17 FDA import refusal record(s) in our database, spanning from 8/29/2007 to 11/5/2024.
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. Laboratorios Combisa S.A. de C.V.'s FEI number is 3003922103.
What types of violations has Laboratorios Combisa S.A. de C.V. received?
Laboratorios Combisa S.A. de C.V. has been cited for 13 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 Laboratorios Combisa S.A. de C.V. come from?
All FDA import refusal data for Laboratorios Combisa S.A. de C.V. 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.