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Freije Quality Engineering, LLC

www.freijequalityengineering.com/

Freije Quality Engineering, LLC, is a full-service consulting firm providing clients with quality system and regulatory affairs consulting. Our goal is to ...

Freijequalityengineering.com

Conversion Technology Metas Server

Freijequalityengineering.com is hosted in United States / Sunnyvale . Freijequalityengineering.com uses HTTPS protocol. Number of used technologies: 5. First technologies: CSS, Html, Iframe, Number of used javascripts: 5. First javascripts: JsNavBarFuncs.js, Globalnavtree.js, Wp_navbar_menub.js, Number of used analytics tools: 0. Its server type is: ATS/5.0.1. Its CMS is: Lexity.

Technologies in use by Freijequalityengineering.com

Technology

Number of occurences: 5

CSS
Html
Iframe
Javascript
Php

Javascripts

Number of occurences: 5

jsNavBarFuncs.js
globalnavtree.js
wp_navbar_menub.js
widgets.js
whv2_001.js

Content Management System

Number of occurences: 1

Lexity

Server Type

ATS/5.0.1

Social

Number of occurences: 1

Twitter Button

Conversion rate optimization
Clickable call number	Not founded!
Conversion form (contact form, subcriber)	Not founded!
Clickable email	Not founded!
CTA (call to action) button	Founded!
List	Not founded!
Image	Not founded!
Enhancement	Not founded!
Responsive website	Founded!
Facebook sharing	Not founded!
Google+ sharing	Not founded!
Twitter sharing	Not founded!
Linkedin sharing	Not founded!
Blog on the webiste	Not founded!

HTTPS (SSL) - Freijequalityengineering.com

SSL certificate

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Meta - Freijequalityengineering.com

Number of occurences: 6

Name:
Content: en-us
Name: Generator
Content: Serif WebPlus X6 (14.0.2.025)
Name: viewport
Content: width=840
Name: keywords
Content: FDA, ISO, Supplier, Supply Chain, Supply Chain Management, Management, Proactive, Quality, Engineering, Quality Engineering, Product, Services, Tier, ASQ, Biomed, Biomedical, Compliance, MWDG, SME, Warning Letter, Remediation, QSR, 21 CFR 820.50, Purchasing Controls, ISO 7.4, ISO 13485, 13485, 820, GMP, GHTF, SG, CAPA, Corrective Action Preventive Action, Corrective Action, Preventive Action, Supplier Controls, Blog, Blogging, Blogger, Veteran, Veteran Owned Business, Supplier Corrective Action Request, SCAR, Supplier Corrective Action, Quality System Regulation, Incoming Inspection, Design Controls, Management Review, cGMP, 820.80, Food and Drug Administration, Food, Drug, Administration, Medical, Device, Medical Devices, FD&C, Food, Drug, and Cosmetic Act, IMDMC, IHIF, IMDRF, 510(k), 483, GHTF, QE, CAPA, Post Market Surveillance, Risk Management, Root Cause, Root Cause Analysis, CQE, CBA, RABQ, Combination Product, insulin pen injector, infusion pump, Freije, Freije Company, The Freije Company, Freije Engineering, Freije Quality Engineering, John Freije, regulatory compliance, regulatory affairs, affairs, Process Validation, VMP, Design, Design Controls, Controls, Process, Process Controls, Medical Device Consulting, Consulting, CDRH, Center for Device and Radiological Health, Transparency, Center, Radiological, Health, CSV, computer system validation, Part 11, recall, post market surveillance, surveillance, post market, class I medical device, class II medical device, PMA, premarket approval, class III medical device, vigilance, post market vigilance, management review, quality audit, acceptance activities, statistics, statistical control, lean, lean manufacturing, SPC, rework, nonconforming product, nonconformance, services, DHF, DHR, DMR, document control, record control, implantable, bone screw, MDD, IVDD, medical device directive, in vitro device directive, directive, CE, CE Mark, NBOG, notify body operations group, supplier quality agreement, quality agreement, SQA, CfPA, production and process controls inspection, measuring, and test equipment, receiving, and process, and finished device acceptance, finished device, finished medical device, device packaging, handling, storage, distribution, installation, device labeling, labeling records device master record, device history records, design history file, quality system requirements, design validation, design review, design transfer, FDA, ISO, Supplier, Supply Chain, Supply Chain Management, Management, Proactive, Quality, Engineering, Quality Engineering, Product, Services, Tier, ASQ, Biomed, Biomedical, Compliance, MWDG, SME, Warning Letter, Remediation, QSR, 21 CFR 820.50, Purchasing Controls, ISO 7.4, ISO 13485, 13485, 820, GMP, GHTF, SG, CAPA, Corrective Action Preventive Action, Corrective Action, Preventive Action, Supplier Controls, Blog, Blogging, Blogger, Veteran, Veteran Owned Business, Supplier Corrective Action Request, SCAR, Supplier Corrective Action, Quality System Regulation, Incoming Inspection, Design Controls, Management Review, cGMP, 820.80, Food and Drug Administration, Food, Drug, Administration, Medical, Device, Medical Devices, FD&C, Food, Drug, and Cosmetic Act, IMDMC, IHIF, IMDRF, 510(k), 483, GHTF, QE, CAPA, Post Market Surveillance, Risk Management, Root Cause, Root Cause Analysis, CQE, CBA, RABQ, Combination Product, insulin pen injector, infusion pump, Freije, Freije Company, The Freije Company, Freije Engineering, Freije Quality Engineering, John Freije, regulatory compliance, regulatory affairs, affairs, Process Validation, VMP, Design, Design Controls, Controls, Process, Process Controls, Medical Device Consulting, Consulting, CDRH, Center for Device and Radiological Health, Transparency, Center, Radiological, Health, CSV, computer system validation, Part 11, recall, post market surveillance, surveillance, post market, class I medical device, class II medical device, PMA, premarket approval, class III medical device, vigilance, post market vigilance, management review, quality audit, acceptance activities, statistics, statistical control, lean, lean manufacturing, SPC, rework, nonconforming product, nonconformance, services, DHF, DHR, DMR, document control, record control, implantable, bone screw, MDD, IVDD, medical device directive, in vitro device directive, directive, CE, CE Mark, NBOG, notify body operations group, supplier quality agreement, quality agreement, SQA, CfPA, production and process controls inspection, measuring, and test equipment, receiving, and process, and finished device acceptance, finished device, finished medical device, device packaging, handling, storage, distribution, installation, device labeling, labeling records device master record, device history records, design history file, quality system requirements, design validation, design review, design transfer
Name: description
Content: Freije Quality Engineering, LLC, is a full-service consulting firm providing clients with quality system and regulatory affairs consulting. Our goal is to make your life easier and your day-to-day operations more efficient.
Name: robots
Content: index,follow

Server / Hosting

IP: 67.195.61.46
Latitude: 37.42
Longitude: -122.01
Country: United States
City: Sunnyvale

Rname

yns1.yahoo.com
yns2.yahoo.com
mx-biz.mail.am0.yahoodns.net

Target

geo-support.yahoo-inc.com

HTTP Header Response

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