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MYLAB DISCOVERY SOLUTIONS

⚠️ Moderate Risk

FEI: 3018707628 • Lonavla • INDIA

FEI

FEI Number

3018707628

📍

Location

Lonavla

🇮🇳

Country

INDIA
🏢

Address

Plot No. 99-B,Lonavla I, , Lonavla, , India

Moderate Risk

FDA Import Risk Assessment

39.3
LowModerateHighCritical

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

Statistics

3
Total Refusals
3
Unique Violations
5/23/2022
Latest Refusal
11/5/2021
Earliest Refusal

Score Breakdown

Violation Severity
68.0×40%
Refusal Volume
22.3×30%
Recency
12.2×20%
Frequency
30.0×10%
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

5083×

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.

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).

Refusal History

DateProductViolationsDivision
5/23/2022
83QKPCORONAVIRUS ANTIGEN DETECTION TEST SYSTEM.
508NO 510(K)
Division of Southeast Imports (DSEI)
2/22/2022
82MZLKIT, TEST, QUALITY CONTROL FOR ENDOTOXIN
508NO 510(K)
Division of Southeast Imports (DSEI)
11/5/2021
83QJRREAGENTS, 2019-NOVEL CORONAVIRUS NUCLEIC ACID
118NOT LISTED
237NO PMA
508NO 510(K)
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is MYLAB DISCOVERY SOLUTIONS's FDA import refusal history?

MYLAB DISCOVERY SOLUTIONS (FEI: 3018707628) has 3 FDA import refusal record(s) in our database, spanning from 11/5/2021 to 5/23/2022.

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. MYLAB DISCOVERY SOLUTIONS's FEI number is 3018707628.

What types of violations has MYLAB DISCOVERY SOLUTIONS received?

MYLAB DISCOVERY SOLUTIONS 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 MYLAB DISCOVERY SOLUTIONS come from?

All FDA import refusal data for MYLAB DISCOVERY SOLUTIONS 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.