SupplierRadar

Laboratorios KEM, S de RL de CV

FDA import alert and refusal historyTijuana, MexicoFEI 3007602386

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Example subjectLaboratorios KEM, S de RL de C added to Import Alert 16-129 (red list)

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As of October 26, 2026, Laboratorios KEM, S de RL de CV is not on any FDA import alert in SupplierRadar's records; FDA refused 7 of its shipment lines between January 16, 2018 and October 23, 2023, most often for required label information not in english (NO ENGLISH).

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

Current status

Import alerts
Not listed
Last import refusal
Zinc (mineral) · UNAPPROVED
Last warning letter
None found
Last inspection
Classified VAI (Voluntary Action Indicated)

Every FDA record for Laboratorios KEM, S de RL de CV

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

2023

  1. Import refusal
    Refused, Zinc (mineral)UNAPPROVEDEntry SCS-0053192-5
    Source
  2. Import refusal
    Refused, Vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c.NO ENGLISHNCONTACTNUTRIT LBLEntry SCS-9112244-3
    Source
  3. Import refusal
    Refused, 4 lines in one entry: L-glutamine (protein); Vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c.NO ENGLISHNCONTACTNUTRIT LBLEntry SCS-8323058-4Show 4 lines
    Source

2021

  1. Inspection
    Inspection classified VAI (Voluntary Action Indicated)Food Composition, Standards, Labeling and Econ
    Source

2018

  1. Inspection
    Inspection classified VAI (Voluntary Action Indicated)Food Composition, Standards, Labeling and Econ
    Source
  2. Import refusal
    Refused, Vitamin, n.e.c.NO ENGLISHEntry UPS-6576838-5
    Source

2012

  1. Inspection
    Inspection classified VAI (Voluntary Action Indicated)Food Composition, Standards, Labeling and Econ
    Source

Refusal charges, in plain English

  • NO ENGLISH6 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.

  • NCONTACT5 refused lines

    No U.S. adverse event contact on supplement label

    The dietary supplement label appeared not to show a U.S. address or phone number through which a serious adverse event can be reported.

  • NUTRIT LBL5 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.

  • UNAPPROVED1 refused line

    Unapproved new drug

    The product appeared to be a new drug within the meaning of section 201(p) of the FD&C Act without an approved New Drug Application. FDA can apply this charge to a food or supplement whose labeling presents it for drug uses.

Questions about Laboratorios KEM, S de RL de CV

Is Laboratorios KEM, S de RL de CV on an FDA import alert?
No listing for Laboratorios KEM, S de RL de CV appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Mexico page.
Has FDA refused shipments from Laboratorios KEM, S de RL de CV?
Yes. FDA refused 7 shipment lines from Laboratorios KEM, S de RL de CV between January 16, 2018 and October 23, 2023. The most recent, on October 23, 2023, was zinc (mineral), charged as UNAPPROVED (unapproved new drug).
Why did FDA refuse Laboratorios KEM, S de RL de CV's shipments?
The most frequent charges are NO ENGLISH (required label information not in english, 6 lines) and NCONTACT (no u.s. adverse event contact on supplement label, 5 lines).
When was Laboratorios KEM, S de RL de CV last inspected by FDA?
FDA's most recent inspection of Laboratorios KEM, S de RL de CV with a final classification is dated September 22, 2021 and was classified VAI (Voluntary Action Indicated).
What is Laboratorios KEM, S de RL de CV's FEI number?
Laboratorios KEM, S de RL de CV's FDA Establishment Identifier (FEI) is 3007602386.

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Example subjectLaboratorios KEM, S de RL de C 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.