Is Laboratorios Funat SAS on an FDA import alert?

No listing for Laboratorios Funat SAS appears in the FDA import alerts SupplierRadar checked on October 25, 2026. Country-wide alerts may still apply to its products; see the Colombia page.

Has FDA refused shipments from Laboratorios Funat SAS?

Yes. FDA refused 4 shipment lines from Laboratorios Funat SAS between December 21, 2017 and April 28, 2025. The most recent, on April 28, 2025, was vitamin, n.e.c., charged as UNAPPROVED (unapproved new drug).

Why did FDA refuse Laboratorios Funat SAS's shipments?

The most frequent charges are UNAPPROVED (unapproved new drug, 4 lines) and NO ENGLISH (required label information not in english, 2 lines).

When was Laboratorios Funat SAS last inspected by FDA?

FDA's most recent inspection of Laboratorios Funat SAS with a final classification is dated April 9, 2019 and was classified VAI (Voluntary Action Indicated).

What is Laboratorios Funat SAS's FEI number?

Laboratorios Funat SAS's FDA Establishment Identifier (FEI) is 3007271231.

Laboratorios Funat SAS

FDA import alert and refusal historySabaneta, ColombiaFEI 3007271231

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As of October 25, 2026, Laboratorios Funat SAS is not on any FDA import alert in SupplierRadar's records; FDA refused 4 of its shipment lines between December 21, 2017 and April 28, 2025, most often for unapproved new drug (UNAPPROVED).

Data from FDA public records, last checked October 25, 2026. Request a correction

Current status

Import alerts: Not listed
Last import refusal: Apr 28, 2025Vitamin, n.e.c. · UNAPPROVED
Last warning letter: None found
Last inspection: Apr 9, 2019Classified VAI (Voluntary Action Indicated)

Every FDA record for Laboratorios Funat SAS

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

2025

Apr 28, 2025Import refusal
Refused, Vitamin, n.e.c.UNAPPROVEDEntry 799-6921767-9
Source

2019

Apr 9, 2019Inspection
Inspection classified VAI (Voluntary Action Indicated)Food Composition, Standards, Labeling and Econ; Foodborne Biological Hazards
Source

2018

Jun 22, 2018Import refusal
Refused, Herbals & botanicals (not teas), n.e.c.UNAPPROVEDEntry UPS-8535031-3
Source

2017

Dec 21, 2017Import refusal
Refused, 2 lines in one entry: Valerian (herbal & botanicals, not teas ii)NO ENGLISHUNAPPROVEDEntry UPS-6320133-0Show 2 linesHide lines
- Refused, Valerian (herbal & botanicals, not teas ii)NO ENGLISH UNAPPROVEDEntry UPS-6320133-0Source
- Refused, Valerian (herbal & botanicals, not teas ii)NO ENGLISH UNAPPROVEDEntry UPS-6320133-0Source
Source

Refusal charges, in plain English

UNAPPROVED4 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.
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.

Questions about Laboratorios Funat SAS

Is Laboratorios Funat SAS on an FDA import alert?: No listing for Laboratorios Funat SAS appears in the FDA import alerts SupplierRadar checked on October 25, 2026. Country-wide alerts may still apply to its products; see the Colombia page.
Has FDA refused shipments from Laboratorios Funat SAS?: Yes. FDA refused 4 shipment lines from Laboratorios Funat SAS between December 21, 2017 and April 28, 2025. The most recent, on April 28, 2025, was vitamin, n.e.c., charged as UNAPPROVED (unapproved new drug).
Why did FDA refuse Laboratorios Funat SAS's shipments?: The most frequent charges are UNAPPROVED (unapproved new drug, 4 lines) and NO ENGLISH (required label information not in english, 2 lines).
When was Laboratorios Funat SAS last inspected by FDA?: FDA's most recent inspection of Laboratorios Funat SAS with a final classification is dated April 9, 2019 and was classified VAI (Voluntary Action Indicated).
What is Laboratorios Funat SAS's FEI number?: Laboratorios Funat SAS's FDA Establishment Identifier (FEI) is 3007271231.

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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.