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Laboratorios Quifarma S.A.

FDA import alert and refusal historySan Miguel Petapa, GuatemalaFEI 3012555420

Recorded by FDA as LABORATORIOS QUIFARMA S.A.

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Example subjectLaboratorios Quifarma S.A added to Import Alert 16-129 (red list)

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As of October 26, 2026, Laboratorios Quifarma S.A. is not on any FDA import alert in SupplierRadar's records; FDA refused 19 of its shipment lines between November 8, 2021 and March 15, 2024, most often for nutrition information missing from label (NUTRIT LBL).

Data from FDA public records, last checked . Request a correction

Current status

Import alerts
Not listed
Last import refusal
Beverage base not mentioned elsewhere, n.e.c. · NUTRIT LBL
Last warning letter
None found
Last inspection
Classified VAI (Voluntary Action Indicated)

Every FDA record for Laboratorios Quifarma S.A.

20 records, newest first. Each line links to the FDA page it came from.

2024

  1. Import refusal
    Refused, Beverage base not mentioned elsewhere, n.e.c.NUTRIT LBLEntry E84-0111379-8
    Source
  2. Import refusal
    Refused, 4 lines in one entry: Soft drinks and waters not mentioned elsewhere, n.e.c.NO ENGLISHNUTRIT LBLEntry E84-0111059-6Show 4 lines
    Source
  3. Import refusal
    Refused, 4 lines in one entry: Beverage base not mentioned elsewhere, n.e.c.NO ENGLISHNUTRIT LBLEntry E84-0111096-8Show 4 lines
    Source
  4. Import refusal
    Refused, 2 lines in one entry: Soft drink, subtropical or tropical fruit flavored, noncarbonated; Soft drink, pit fruit flavored, noncarbonatedNO ENGLISHNUTRIT LBLEntry U10-1231423-7Show 2 lines
    Source
  5. Import refusal
    Refused, 4 lines in one entry: Soft drinks and waters not mentioned elsewhere, n.e.c.COLORLABELNUTRIT LBLHEALTH CEntry E84-0110200-7Show 4 lines
    Source

2021

  1. Import refusal
    Refused, 4 lines in one entry: Soft drink, subtropical or tropical fruit flavored, carbonatedSTD FILLLABELINGEntry E84-0099052-7Show 4 lines
    Source

2018

  1. Inspection
    Inspection classified VAI (Voluntary Action Indicated)Foodborne Biological Hazards
    Source

Refusal charges, in plain English

  • NUTRIT LBL15 refused lines

    Nutrition information missing from label

    The label or labeling appeared not to carry the nutrition information that U.S. law requires for the food.

  • NO ENGLISH10 refused lines

    Required label information not in English

    Information that must appear on the label appeared not to be given in English, or not to be repeated in every language used on the label.

  • HEALTH C4 refused lines

    Unauthorized nutrient content or health claim

    The label or labeling appeared to carry a nutrient content claim or health claim that is not authorized.

  • LABELING4 refused lines

    Fair Packaging and Labeling Act

    The package appeared not to meet the Fair Packaging and Labeling Act because of the placement, form, or contents of a required label statement.

  • STD FILL4 refused lines

    STD FILL

  • COLORLABEL3 refused lines

    Required information not prominent

    Information required on the label appeared not to be placed prominently enough, or in such terms, to be read and understood by an ordinary consumer.

Questions about Laboratorios Quifarma S.A.

Is Laboratorios Quifarma S.A. on an FDA import alert?
No listing for Laboratorios Quifarma S.A. appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Guatemala page.
Has FDA refused shipments from Laboratorios Quifarma S.A.?
Yes. FDA refused 19 shipment lines from Laboratorios Quifarma S.A. between November 8, 2021 and March 15, 2024. The most recent, on March 15, 2024, was beverage base not mentioned elsewhere, n.e.c., charged as NUTRIT LBL (nutrition information missing from label).
Why did FDA refuse Laboratorios Quifarma S.A.'s shipments?
The most frequent charges are NUTRIT LBL (nutrition information missing from label, 15 lines) and NO ENGLISH (required label information not in english, 10 lines).
When was Laboratorios Quifarma S.A. last inspected by FDA?
FDA's most recent inspection of Laboratorios Quifarma S.A. with a final classification is dated August 29, 2018 and was classified VAI (Voluntary Action Indicated).
What is Laboratorios Quifarma S.A.'s FEI number?
Laboratorios Quifarma S.A.'s FDA Establishment Identifier (FEI) is 3012555420.

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Example subjectLaboratorios Quifarma S.A added to Import Alert 16-129 (red list)

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SupplierRadar is not affiliated with the U.S. Food and Drug Administration. Data comes from public FDA records and may contain errors. This is not legal advice; importers remain responsible for their supplier evaluations.