LABORATORIOS QUIFARMA S.A.
⚠️ Moderate Risk
FEI: 3012555420 • San Miguel Petapa, Guatemala • GUATEMALA
FEI Number
3012555420
Location
San Miguel Petapa, Guatemala
Country
GUATEMALAAddress
Km 17.5 Road To a Villa Canales, , San Miguel Petapa, Guatemala, Guatemala
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
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.
NO ENGLISH
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)).
STD FILL
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(h)(2) of the FD&C Act in that the article purports to be or is represented as a food for which a standard or standards of fill of container have been prescribed by regulations as provided by Section 401 of the FD&C Act and the article falls below the applicable standard of fill and its label does not bear a statement that it falls below such standard in such manner and form as such regulations specify.
LABELING
The article appears in violation of FPLA because of its placement, form and/or contents statement.
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.
COLORLABEL
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.
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.
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).
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).
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 3/15/2024 | 30YYT99BEVERAGE BASE NOT MENTIONED ELSEWHERE, N.E.C. | 482NUTRIT LBL | Division of Southeast Imports (DSEI) |
| 3/15/2024 | 29YYT99SOFT DRINKS AND WATERS NOT MENTIONED ELSEWHERE, N.E.C. | Division of Southeast Imports (DSEI) | |
| 3/15/2024 | 29YYT99SOFT DRINKS AND WATERS NOT MENTIONED ELSEWHERE, N.E.C. | Division of Southeast Imports (DSEI) | |
| 3/15/2024 | 29YYT99SOFT DRINKS AND WATERS NOT MENTIONED ELSEWHERE, N.E.C. | Division of Southeast Imports (DSEI) | |
| 3/15/2024 | 29YYT99SOFT DRINKS AND WATERS NOT MENTIONED ELSEWHERE, N.E.C. | Division of Southeast Imports (DSEI) | |
| 2/12/2024 | 30YYT99BEVERAGE BASE NOT MENTIONED ELSEWHERE, N.E.C. | Division of Southeast Imports (DSEI) | |
| 2/12/2024 | 30YYT99BEVERAGE BASE NOT MENTIONED ELSEWHERE, N.E.C. | Division of Southeast Imports (DSEI) | |
| 2/12/2024 | 30YYT99BEVERAGE BASE NOT MENTIONED ELSEWHERE, N.E.C. | Division of Southeast Imports (DSEI) | |
| 2/12/2024 | 30YYT99BEVERAGE BASE NOT MENTIONED ELSEWHERE, N.E.C. | Division of Southeast Imports (DSEI) | |
| 1/22/2024 | 29AGT07SOFT DRINK, SUBTROPICAL OR TROPICAL FRUIT FLAVORED, NONCARBONATED | Division of Southeast Imports (DSEI) | |
| 1/22/2024 | 29AGT05SOFT DRINK, PIT FRUIT FLAVORED, NONCARBONATED | Division of Southeast Imports (DSEI) | |
| 1/5/2024 | 29YYT99SOFT DRINKS AND WATERS NOT MENTIONED ELSEWHERE, N.E.C. | Division of Southeast Imports (DSEI) | |
| 1/5/2024 | 29YYT99SOFT DRINKS AND WATERS NOT MENTIONED ELSEWHERE, N.E.C. | Division of Southeast Imports (DSEI) | |
| 1/5/2024 | 29YYT99SOFT DRINKS AND WATERS NOT MENTIONED ELSEWHERE, N.E.C. | Division of Southeast Imports (DSEI) | |
| 1/5/2024 | 29YYT99SOFT DRINKS AND WATERS NOT MENTIONED ELSEWHERE, N.E.C. | Division of Southeast Imports (DSEI) | |
| 11/8/2021 | 29BGT07SOFT DRINK, SUBTROPICAL OR TROPICAL FRUIT FLAVORED, CARBONATED | Division of Southeast Imports (DSEI) | |
| 11/8/2021 | 29BGT07SOFT DRINK, SUBTROPICAL OR TROPICAL FRUIT FLAVORED, CARBONATED | Division of Southeast Imports (DSEI) | |
| 11/8/2021 | 29BGT07SOFT DRINK, SUBTROPICAL OR TROPICAL FRUIT FLAVORED, CARBONATED | Division of Southeast Imports (DSEI) | |
| 11/8/2021 | 29BGT07SOFT DRINK, SUBTROPICAL OR TROPICAL FRUIT FLAVORED, CARBONATED | Division of Southeast Imports (DSEI) | |
| 6/17/2020 | 56ECE80TETRACYCLINE (TETRACYCLINES) | 75UNAPPROVED | Division of Southeast Imports (DSEI) |
| 6/23/2008 | 41GCB03ORAL REHYDRATION PRODUCTS | Division of Southeast Imports (DSEI) |
Frequently Asked Questions
What is LABORATORIOS QUIFARMA S.A.'s FDA import refusal history?
LABORATORIOS QUIFARMA S.A. (FEI: 3012555420) has 21 FDA import refusal record(s) in our database, spanning from 6/23/2008 to 3/15/2024.
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 QUIFARMA S.A.'s FEI number is 3012555420.
What types of violations has LABORATORIOS QUIFARMA S.A. received?
LABORATORIOS QUIFARMA S.A. has been cited for 9 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 QUIFARMA S.A. come from?
All FDA import refusal data for LABORATORIOS QUIFARMA 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.