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FOREST HILLS LAB KOREA

⚠️ Moderate Risk

FEI: 3039304433 • Anyang, Gyeonggi • SOUTH KOREA

FEI

FEI Number

3039304433

📍

Location

Anyang, Gyeonggi

🇰🇷
🏢

Address

706 707 O Biz Tower, Dongan District, Anyang, Gyeonggi, South Korea

Moderate Risk

FDA Import Risk Assessment

45.6
LowModerateHighCritical

This firm has a moderate history of FDA import refusals. Some attention may be warranted.

Statistics

1
Total Refusals
5
Unique Violations
9/29/2025
Latest Refusal
9/29/2025
Earliest Refusal

Score Breakdown

Violation Severity
56.0×40%
Refusal Volume
11.2×30%
Recency
94.2×20%
Frequency
10.0×10%
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

1181×

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).

2371×

NO PMA

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the device appears to be a Class III device and does not appear to have in effect an approved application for premarket approval pursuant to Section 515 of the Act, or an exemption pursuant to Section 520(g)(1).

32801×

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.

3411×

REGISTERED

It appears the device is subject to listing under 510(j) and the initial distributor has not registered as required by 21 CFR 807.20 (a)(5).

841×

RX DEVICE

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it is a prescription device that appears to not feature a prescription device legend as required by 21 CFR 801.109.

Refusal History

DateProductViolationsDivision
9/29/2025
79LMHIMPLANT, DERMAL, COLLAGEN FOR AESTHETIC USE
118NOT LISTED
237NO PMA
3280FRNMFGREG
341REGISTERED
84RX DEVICE
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is FOREST HILLS LAB KOREA's FDA import refusal history?

FOREST HILLS LAB KOREA (FEI: 3039304433) has 1 FDA import refusal record(s) in our database, spanning from 9/29/2025 to 9/29/2025.

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. FOREST HILLS LAB KOREA's FEI number is 3039304433.

What types of violations has FOREST HILLS LAB KOREA received?

FOREST HILLS LAB KOREA has been cited for 5 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 FOREST HILLS LAB KOREA come from?

All FDA import refusal data for FOREST HILLS LAB KOREA 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.