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Precis Technologies

⚠️ Moderate Risk

FEI: 3010583955 • Punjab • PAKISTAN

FEI

FEI Number

3010583955

📍

Location

Punjab

🇵🇰

Country

PAKISTAN
🏢

Address

Sialkot 51310, , Punjab, , Pakistan

Moderate Risk

FDA Import Risk Assessment

43.8
LowModerateHighCritical

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

Statistics

4
Total Refusals
1
Unique Violations
2/3/2014
Latest Refusal
2/3/2014
Earliest Refusal

Score Breakdown

Violation Severity
80.0×40%
Refusal Volume
25.9×30%
Recency
0.0×20%
Frequency
40.0×10%
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

2904×

DE IMP GMP

The article is subject to refusal of admission pursuant to section 801(a)(1) in that it appears that the methods used in, or the facilities or controls used for, the manufacture of the device do not conform to the applicable requirements of section 520(f).

Refusal History

DateProductViolationsDivision
2/3/2014
76EKBEXPLORER, OPERATIVE
290DE IMP GMP
Cincinnati District Office (CIN-DO)
2/3/2014
76EMACEMENT, DENTAL
290DE IMP GMP
Cincinnati District Office (CIN-DO)
2/3/2014
76EJBHANDLE, INSTRUMENT, DENTAL
290DE IMP GMP
Cincinnati District Office (CIN-DO)
2/3/2014
76EMGFORCEPS, TOOTH EXTRACTOR, SURGICAL
290DE IMP GMP
Cincinnati District Office (CIN-DO)

Frequently Asked Questions

What is Precis Technologies's FDA import refusal history?

Precis Technologies (FEI: 3010583955) has 4 FDA import refusal record(s) in our database, spanning from 2/3/2014 to 2/3/2014.

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. Precis Technologies's FEI number is 3010583955.

What types of violations has Precis Technologies received?

Precis Technologies has been cited for 1 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 Precis Technologies come from?

All FDA import refusal data for Precis Technologies 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.