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 > FDAnews Device Daily Bulletin > FDA Warns Aesculap for Reporting, Procedural Failures

FDAnews Device Daily Bulletin

Nov. 4, 2011 | Vol. 8 No. 217

FDA Warns Aesculap for Reporting, Procedural Failures

The FDA warned German devicemaker Aesculap AG for failing to conduct investigations after receiving multiple consumer complaints.
The GMP Letter

Register Now
Print This Page
Email This Article
RSS
Archives

Related Articles

Maker of Radioactive Needle Sets Warned Over Complaint Handling Speech Therapy Devicemakers Warned Over Quality System Shortfalls Industry: Trans-Tasman Warning System Could Spark Unnecessary Concerns Baxter Warned for Pump Change Without Proper Notification

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.