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 SubmissionPosted: 06/15/2012
ID: FDA-2012-N-0477-0002
Jul 23,2012 11:59 PM ET
Anonymous - Comment Public SubmissionPosted: 07/23/2012
ID: FDA-2012-N-0477-0003
Anonymous - Comment
This is comment on Notice
Agency Information Collection Activities; Proposed Collection, Comment Request; Investigational Device Exemptions Reports and Records
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Related Comments
Public Submission Posted: 06/15/2012 ID: FDA-2012-N-0477-0002
Jul 23,2012 11:59 PM ET
Public Submission Posted: 07/23/2012 ID: FDA-2012-N-0477-0003
Jul 23,2012 11:59 PM ET