ImportRefusal LogoImportRefusal

LABORATORIOS QUIFARMA S.A.

⚠️ Moderate Risk

FEI: 3012555420 • San Miguel Petapa, Guatemala • GUATEMALA

FEI

FEI Number

3012555420

📍

Location

San Miguel Petapa, Guatemala

🇬🇹

Country

GUATEMALA
🏢

Address

Km 17.5 Road To a Villa Canales, , San Miguel Petapa, Guatemala, Guatemala

Moderate Risk

FDA Import Risk Assessment

45.6
LowModerateHighCritical

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

Statistics

21
Total Refusals
9
Unique Violations
3/15/2024
Latest Refusal
6/23/2008
Earliest Refusal

Score Breakdown

Violation Severity
41.6×40%
Refusal Volume
49.7×30%
Recency
63.5×20%
Frequency
13.3×10%
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

48215×

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.

32411×

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)).

2554×

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.

4734×

LABELING

The article appears in violation of FPLA because of its placement, form and/or contents statement.

4884×

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.

38653×

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.

831×

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.

621×

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).

751×

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

DateProductViolationsDivision
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.
324NO ENGLISH
482NUTRIT LBL
Division of Southeast Imports (DSEI)
3/15/2024
29YYT99SOFT DRINKS AND WATERS NOT MENTIONED ELSEWHERE, N.E.C.
324NO ENGLISH
482NUTRIT LBL
Division of Southeast Imports (DSEI)
3/15/2024
29YYT99SOFT DRINKS AND WATERS NOT MENTIONED ELSEWHERE, N.E.C.
324NO ENGLISH
482NUTRIT LBL
Division of Southeast Imports (DSEI)
3/15/2024
29YYT99SOFT DRINKS AND WATERS NOT MENTIONED ELSEWHERE, N.E.C.
324NO ENGLISH
482NUTRIT LBL
Division of Southeast Imports (DSEI)
2/12/2024
30YYT99BEVERAGE BASE NOT MENTIONED ELSEWHERE, N.E.C.
324NO ENGLISH
482NUTRIT LBL
Division of Southeast Imports (DSEI)
2/12/2024
30YYT99BEVERAGE BASE NOT MENTIONED ELSEWHERE, N.E.C.
324NO ENGLISH
482NUTRIT LBL
Division of Southeast Imports (DSEI)
2/12/2024
30YYT99BEVERAGE BASE NOT MENTIONED ELSEWHERE, N.E.C.
324NO ENGLISH
482NUTRIT LBL
Division of Southeast Imports (DSEI)
2/12/2024
30YYT99BEVERAGE BASE NOT MENTIONED ELSEWHERE, N.E.C.
324NO ENGLISH
482NUTRIT LBL
Division of Southeast Imports (DSEI)
1/22/2024
29AGT07SOFT DRINK, SUBTROPICAL OR TROPICAL FRUIT FLAVORED, NONCARBONATED
324NO ENGLISH
482NUTRIT LBL
Division of Southeast Imports (DSEI)
1/22/2024
29AGT05SOFT DRINK, PIT FRUIT FLAVORED, NONCARBONATED
324NO ENGLISH
482NUTRIT LBL
Division of Southeast Imports (DSEI)
1/5/2024
29YYT99SOFT DRINKS AND WATERS NOT MENTIONED ELSEWHERE, N.E.C.
3865COLORLABEL
482NUTRIT LBL
488HEALTH C
Division of Southeast Imports (DSEI)
1/5/2024
29YYT99SOFT DRINKS AND WATERS NOT MENTIONED ELSEWHERE, N.E.C.
3865COLORLABEL
482NUTRIT LBL
488HEALTH C
Division of Southeast Imports (DSEI)
1/5/2024
29YYT99SOFT DRINKS AND WATERS NOT MENTIONED ELSEWHERE, N.E.C.
3865COLORLABEL
482NUTRIT LBL
488HEALTH C
Division of Southeast Imports (DSEI)
1/5/2024
29YYT99SOFT DRINKS AND WATERS NOT MENTIONED ELSEWHERE, N.E.C.
482NUTRIT LBL
488HEALTH C
Division of Southeast Imports (DSEI)
11/8/2021
29BGT07SOFT DRINK, SUBTROPICAL OR TROPICAL FRUIT FLAVORED, CARBONATED
255STD FILL
473LABELING
Division of Southeast Imports (DSEI)
11/8/2021
29BGT07SOFT DRINK, SUBTROPICAL OR TROPICAL FRUIT FLAVORED, CARBONATED
255STD FILL
473LABELING
Division of Southeast Imports (DSEI)
11/8/2021
29BGT07SOFT DRINK, SUBTROPICAL OR TROPICAL FRUIT FLAVORED, CARBONATED
255STD FILL
473LABELING
Division of Southeast Imports (DSEI)
11/8/2021
29BGT07SOFT DRINK, SUBTROPICAL OR TROPICAL FRUIT FLAVORED, CARBONATED
255STD FILL
473LABELING
Division of Southeast Imports (DSEI)
6/17/2020
56ECE80TETRACYCLINE (TETRACYCLINES)
75UNAPPROVED
Division of Southeast Imports (DSEI)
6/23/2008
41GCB03ORAL REHYDRATION PRODUCTS
324NO ENGLISH
62NEEDS FCE
83NO PROCESS
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.