Anonymous - Comment

Document ID: FDA-2012-N-0477-0002
Document Type: Public Submission
Agency: Food And Drug Administration
Received Date: May 26 2012, at 12:00 AM Eastern Daylight Time
Date Posted: June 15 2012, at 12:00 AM Eastern Standard Time
Comment Start Date: May 24 2012, at 12:00 AM Eastern Standard Time
Comment Due Date: July 23 2012, at 11:59 PM Eastern Standard Time
Tracking Number: 8101e49e
View Document:  View as format xml

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omb 0910-0078 all medical devices/products should be tested in the usa if they are to be sold in the usa. the usa should accept no tests done in any other country. all tests should be onpeople or in lab dishes, no animals should be usted in any testing. such testing has no relevance. testing out of this country is slipper, fakery, fraud, negligent and outright deception of american regulation. i do not believe fda does enough due diligence inspections of such reports submitted by profiteers. there is no purpose to the reports if fda is so sloppy when examiining them. fda has made alot of boners lately in approving all kinds of products that did more harm than good. first do no harm. we need new management at the fda to get more diligence from the staff employees, who seem to be extremely sloppy in their work. the public is being shortchanged by fda and is not being protected at all. the public is dying and being injured by sloppy fda work.

Related Comments

   
Total: 2
Anonymous - Comment
Public Submission    Posted: 06/15/2012     ID: FDA-2012-N-0477-0002

Jul 23,2012 11:59 PM ET
Anonymous - Comment
Public Submission    Posted: 07/23/2012     ID: FDA-2012-N-0477-0003

Jul 23,2012 11:59 PM ET