Is Laboratorios Vijosa, S.A. de C.V. on an FDA import alert?

No listing for Laboratorios Vijosa, S.A. de C.V. appears in the FDA import alerts SupplierRadar checked on October 27, 2026. Country-wide alerts may still apply to its products; see the El Salvador page.

Has FDA refused shipments from Laboratorios Vijosa, S.A. de C.V.?

Yes. FDA refused 8 shipment lines from Laboratorios Vijosa, S.A. de C.V. between September 17, 2018 and August 31, 2026. The most recent, on August 31, 2026, was vitamin k (phytonadione), charged as NOT LISTED (product not listed with fda).

Why did FDA refuse Laboratorios Vijosa, S.A. de C.V.'s shipments?

The most frequent charges are UNAPPROVED (unapproved new drug, 6 lines) and NOT LISTED (product not listed with fda, 3 lines).

What is Laboratorios Vijosa, S.A. de C.V.'s FEI number?

Laboratorios Vijosa, S.A. de C.V.'s FDA Establishment Identifier (FEI) is 3013300201.

Laboratorios Vijosa, S.A. de C.V.

FDA import alert and refusal historyAntiguo Cuscatlan, El SalvadorFEI 3013300201

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As of October 27, 2026, Laboratorios Vijosa, S.A. de C.V. is not on any FDA import alert in SupplierRadar's records; FDA refused 8 of its shipment lines between September 17, 2018 and August 31, 2026, most often for unapproved new drug (UNAPPROVED).

Data from FDA public records, last checked October 27, 2026. Request a correction

Current status

Import alerts: Not listed
Last import refusal: Aug 31, 2026Vitamin k (phytonadione) · NOT LISTED
Last warning letter: None found
Last inspection: None on record

Every FDA record for Laboratorios Vijosa, S.A. de C.V.

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

2026

Aug 31, 2026Import refusal
Refused, Vitamin k (phytonadione)NOT LISTED FRNMFGREG UNAPPROVED RX LEGENDEntry 1FX-8856869-6
Source

2025

Sep 29, 2025Import refusal
Refused, 2 lines in one entry: Vitamin b1 (thiamine)NOT LISTEDUNAPPROVEDEntry AEK-7624250-0Show 2 linesHide lines
- Refused, Vitamin b1 (thiamine)NOT LISTED UNAPPROVEDEntry AEK-7624250-0Source
- Refused, Vitamin b1 (thiamine)NOT LISTED UNAPPROVEDEntry AEK-7624250-0Source
Source
Sep 24, 2025Import refusal
Refused, Vitamin d2 (calciferol)UNAPPROVEDEntry AEK-7567983-5
Source

2023

Mar 28, 2023Import refusal
Refused, Glucosamine sulfate (herbal and botanicals, not teas ii)UNAPPROVEDEntry AEK-2793558-2
Source

2022

Aug 25, 2022Import refusal
Refused, Vitamin, n.e.c.LIST INGRE NO ENGLISH NUTRIT LBL UNAPPROVEDEntry 960-0253304-8
Source

2019

Jun 24, 2019Import refusal
Refused, Multiple vitamins (mvi-12 vitamin combo) (vitamin)NO ENGLISHEntry B4Y-0009933-5
Source

2018

Sep 17, 2018Import refusal
Refused, Vitamin b1 (thiamine)DIETARYING NUTRIT LBLEntry B4Y-0007239-9
Source

Refusal charges, in plain English

UNAPPROVED6 refused lines
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.
NOT LISTED3 refused lines
Product not listed with FDA
The product appeared to be a drug or device that is not included in the listing FDA requires under section 510(j) of the FD&C Act.
NO ENGLISH2 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.
NUTRIT LBL2 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.
DIETARYING1 refused line
Dietary ingredients not listed
The dietary supplement label appeared not to list each dietary ingredient and its quantity, or the total quantity of a proprietary blend.
FRNMFGREG1 refused line
FRNMFGREG
LIST INGRE1 refused line
Ingredients not listed
The product is made from two or more ingredients and the label appeared not to list the common or usual name of each one (or, for a juice beverage, the percentage of juice).
RX LEGEND1 refused line
RX LEGEND

Questions about Laboratorios Vijosa, S.A. de C.V.

Is Laboratorios Vijosa, S.A. de C.V. on an FDA import alert?: No listing for Laboratorios Vijosa, S.A. de C.V. appears in the FDA import alerts SupplierRadar checked on October 27, 2026. Country-wide alerts may still apply to its products; see the El Salvador page.
Has FDA refused shipments from Laboratorios Vijosa, S.A. de C.V.?: Yes. FDA refused 8 shipment lines from Laboratorios Vijosa, S.A. de C.V. between September 17, 2018 and August 31, 2026. The most recent, on August 31, 2026, was vitamin k (phytonadione), charged as NOT LISTED (product not listed with fda).
Why did FDA refuse Laboratorios Vijosa, S.A. de C.V.'s shipments?: The most frequent charges are UNAPPROVED (unapproved new drug, 6 lines) and NOT LISTED (product not listed with fda, 3 lines).
What is Laboratorios Vijosa, S.A. de C.V.'s FEI number?: Laboratorios Vijosa, S.A. de C.V.'s FDA Establishment Identifier (FEI) is 3013300201.

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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.