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Laboratorios Andromaco S.A.

⚠️ High Risk

FEI: 3008089871 • Penalolen • CHILE

FEI

FEI Number

3008089871

📍

Location

Penalolen

🇨🇱

Country

CHILE
🏢

Address

Penalolen, Avenida Quilin 5273, Penalolen, , Chile

High Risk

FDA Import Risk Assessment

55.2
LowModerateHighCritical

This firm has a significant history of FDA import refusals with notable violations.

Statistics

8
Total Refusals
3
Unique Violations
1/2/2025
Latest Refusal
10/5/2015
Earliest Refusal

Score Breakdown

Violation Severity
76.7×40%
Refusal Volume
35.3×30%
Recency
65.3×20%
Frequency
8.7×10%
How is this score calculated?

Proprietary Algorithm

  • 40% Violation Severity — AI-assessed (1-10)
  • 30% Refusal Volume — Logarithmic scale
  • 20% Recency — Decays over 5 years
  • 10% Frequency — Refusals per year

© ImportRefusal.com Original Analysis

Violation Summary

758×

UNAPPROVED

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be a new drug within the meaning of Section 201(p) without an approved New Drug Application (NDA).

1182×

NOT LISTED

It appears the drug or device is not included in a list required by Section 510(j), or a notice or other information respecting it was not provided as required by section 510(j) or 510(k).

32802×

FRNMFGREG

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to be misbranded as defined in section 502(o) of the FD&C Act. It appears that it was manufactured, prepared, propagated, compounded, or processed in an establishment not duly registered under section 510 of the Act.

Refusal History

DateProductViolationsDivision
1/2/2025
60LAY01ACETAMINOPHEN (ANALGESIC)
118NOT LISTED
3280FRNMFGREG
75UNAPPROVED
Division of Southeast Imports (DSEI)
6/2/2020
64SDA29ZOPICLONE
75UNAPPROVED
Division of Southeast Imports (DSEI)
2/2/2017
63HDY10LACTULOSE (CATHARTIC)
75UNAPPROVED
New Orleans District Office (NOL-DO)
2/2/2017
62KDY10OMEPRAZOLE (ANTI-PERISTALTIC, ANTI-DIARRHEAL)
75UNAPPROVED
New Orleans District Office (NOL-DO)
2/2/2017
64BDY37SPIRONOLACTONE (DIURETIC)
75UNAPPROVED
New Orleans District Office (NOL-DO)
2/2/2017
64NDY06FERROUS SULFATE (HEMATINIC)
75UNAPPROVED
New Orleans District Office (NOL-DO)
2/2/2017
54ABY13VITAMIN C (ASCORBIC ACID)
75UNAPPROVED
New Orleans District Office (NOL-DO)
10/5/2015
64GDA07ESTRADIOL (ESTROGEN)
118NOT LISTED
3280FRNMFGREG
75UNAPPROVED
Florida District Office (FLA-DO)

Frequently Asked Questions

What is Laboratorios Andromaco S.A.'s FDA import refusal history?

Laboratorios Andromaco S.A. (FEI: 3008089871) has 8 FDA import refusal record(s) in our database, spanning from 10/5/2015 to 1/2/2025.

What is an FEI number?

FEI stands for Firm Establishment Identifier. It's a unique number assigned by the FDA to identify establishments that manufacture, process, pack, or hold food, drugs, medical devices, or other FDA-regulated products. Laboratorios Andromaco S.A.'s FEI number is 3008089871.

What types of violations has Laboratorios Andromaco S.A. received?

Laboratorios Andromaco S.A. has been cited for 3 different violation type(s). Common FDA violations include adulteration (unsafe or unsanitary products), misbranding (incorrect or misleading labels), and regulatory non-compliance.

Where does this information about Laboratorios Andromaco S.A. come from?

All FDA import refusal data for Laboratorios Andromaco S.A. is sourced from the official FDA Data Dashboard (datadashboard.fda.gov), a public government database maintained by the U.S. Food and Drug Administration.

Data sourced from the FDA Data Dashboard, a public database maintained by the U.S. Food and Drug Administration.