Your shopping cart is empty

Subscriber login

REGISTER FOR FREE EZINES

Advanced Search

Home
Books
Conferences
DVDs
Newsletters
Form 483s
Pharma Quality Advisor
Webinar Training Pass
White Papers
Advertising/Sponsorships
About Us

E-Zines

Check out our free and informative ezines and sign up now

Home > Newsletters > Devices & Diagnostics Letter > Impact Instrumentation Form 483 Details Quality Control Issues

Devices & Diagnostics Letter

Sept. 19, 2011 | Vol. 38 No. 37

Impact Instrumentation Form 483 Details Quality Control Issues

Impact Instrumentation didn’t identify or repair flaws leaving nonconformities in finished or in-process devices, according to a recent Form 483.

This article is viewable by subscribers only. To view this article, please select an option below.

Subscribe
Print This Page
RSS
Free Trial
Archives
Sample PDF

Related Articles

Supplier Monitoring, Tight Quality Agreement Keep Changes in Check FDA Warns Epimed International for Supplier Control, Procedural Issues FDA Expert: Trust Gut Instincts As First Supplier Qualification Step TCM Warned Over Lax Supplier Controls, GMPs

Home
Advertising/Sponsorships
About Us
Contact Us
Site Map
Privacy Policy

300 N. Washington St., Suite 200, Falls Church, VA 22046, USA.
Phone (703) 538-7600 - Fax (703) 538-7676 - Toll free (888) 838-5578.

ePublishing :: CMS, Hosting & Web Development | © Copyright by FDAnews

All rights reserved. Do not duplicate or redistribute in any form.