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 > Medrad Warning Cites Failure to File Corrections Report

Devices & Diagnostics Letter

May 30, 2011 | Vol. 38 No. 22

Medrad Warning Cites Failure to File Corrections Report

The FDA has warned Medrad saying there is no evidence the company submitted a correction and removal report for several corrections to a product.

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

Inadequate GMPs Garner Warning Letter for Italian Devicemaker Cat on Premises Helps Land Devicemaker a Form 483 Keystone Gets Warning After FDA Finds Wooden Sticks Used in Drug Manufacture Cosmetic Devices Company Warned on Misleading Website Promotions

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.