Laboratorio Adromaco
FDA import alert and refusal historySantiago, ChileFEI 3013143982
Recorded by FDA as LABORATORIO ADROMACO
As of October 26, 2026, Laboratorio Adromaco is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on February 2, 2017, 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 c (ascorbic acid) · UNAPPROVED
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Laboratorio Adromaco
1 record, newest first. Each line links to the FDA page it came from.
2017
- Import refusalRefused, Vitamin c (ascorbic acid)UNAPPROVEDEntry 799-8951051-1Source
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 Laboratorio Adromaco
- Is Laboratorio Adromaco on an FDA import alert?
- No listing for Laboratorio Adromaco 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 Laboratorio Adromaco?
- Yes. FDA refused 1 shipment line from Laboratorio Adromaco on February 2, 2017. The most recent, on February 2, 2017, was vitamin c (ascorbic acid), charged as UNAPPROVED (unapproved new drug).
- Why did FDA refuse Laboratorio Adromaco's shipments?
- The most frequent charge is UNAPPROVED (unapproved new drug, 1 line).
- What is Laboratorio Adromaco's FEI number?
- Laboratorio Adromaco's FDA Establishment Identifier (FEI) is 3013143982.
Buying from Laboratorio Adromaco?
Watch it and get the FDA record the day it changes. Free for one supplier.
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.