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Esg Panatec

⚠️ Moderate Risk

FEI: 3006681129 • Muke Kuning Batam 29433 • INDONESIA

FEI

FEI Number

3006681129

📍

Location

Muke Kuning Batam 29433

🇮🇩

Country

INDONESIA
🏢

Address

Batamindo Industrial Park, , Muke Kuning Batam 29433, , Indonesia

Moderate Risk

FDA Import Risk Assessment

33.5
LowModerateHighCritical

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

Statistics

5
Total Refusals
5
Unique Violations
7/24/2012
Latest Refusal
11/15/2010
Earliest Refusal

Score Breakdown

Violation Severity
54.6×40%
Refusal Volume
28.8×30%
Recency
0.0×20%
Frequency
29.6×10%
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

3414×

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).

1183×

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).

2373×

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).

5082×

NO 510(K)

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it is a post 1976 device for which a Section 510(k)application does not appear to have been determined substantially equivalent or otherwise filed.

4761×

NO REGISTR

The article appears to be an electronic product that does not comply with an applicable standard as prescribed by Section 534 because no reporting has been provided as required by Section 537(b).

Refusal History

DateProductViolationsDivision
7/24/2012
89NZFMASSAGER, COSMETIC, STATIC ELECTRICITY-EMITTING
118NOT LISTED
237NO PMA
341REGISTERED
Southwest Import District Office (SWI-DO)
6/18/2012
89ISAMASSAGER, THERAPEUTIC, ELECTRIC
237NO PMA
341REGISTERED
508NO 510(K)
Southwest Import District Office (SWI-DO)
6/18/2012
89ISAMASSAGER, THERAPEUTIC, ELECTRIC
237NO PMA
341REGISTERED
508NO 510(K)
Southwest Import District Office (SWI-DO)
8/4/2011
89ISAMASSAGER, THERAPEUTIC, ELECTRIC
118NOT LISTED
476NO REGISTR
Los Angeles District Office (LOS-DO)
11/15/2010
89NZFMASSAGER, COSMETIC, STATIC ELECTRICITY-EMITTING
118NOT LISTED
341REGISTERED
Southwest Import District Office (SWI-DO)

Frequently Asked Questions

What is Esg Panatec's FDA import refusal history?

Esg Panatec (FEI: 3006681129) has 5 FDA import refusal record(s) in our database, spanning from 11/15/2010 to 7/24/2012.

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. Esg Panatec's FEI number is 3006681129.

What types of violations has Esg Panatec received?

Esg Panatec 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 Esg Panatec come from?

All FDA import refusal data for Esg Panatec 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.