SupplierRadar

Chilean Laboratory

FDA import alert and refusal historySantiago, ChileFEI 3036520254

Recorded by FDA as CHILEAN LABORATORY

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Example subjectChilean Laborator added to Import Alert 16-129 (red list)

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As of October 26, 2026, Chilean Laboratory is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on September 24, 2025, most often for unapproved new drug (UNAPPROVED).

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

Current status

Import alerts
Not listed
Last import refusal
Vitamin, n.e.c. · UNAPPROVED
Last warning letter
None found
Last inspection
None on record

Every FDA record for Chilean Laboratory

1 record, newest first. Each line links to the FDA page it came from.

2025

  1. Import refusal
    Refused, Vitamin, n.e.c.UNAPPROVEDEntry AEK-7567983-5
    Source

Refusal charges, in plain English

  • 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 Chilean Laboratory

Is Chilean Laboratory on an FDA import alert?
No listing for Chilean Laboratory appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Chile page.
Has FDA refused shipments from Chilean Laboratory?
Yes. FDA refused 1 shipment line from Chilean Laboratory on September 24, 2025. The most recent, on September 24, 2025, was vitamin, n.e.c., charged as UNAPPROVED (unapproved new drug).
Why did FDA refuse Chilean Laboratory's shipments?
The most frequent charge is UNAPPROVED (unapproved new drug, 1 line).
What is Chilean Laboratory's FEI number?
Chilean Laboratory's FDA Establishment Identifier (FEI) is 3036520254.

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Example subjectChilean Laborator 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.