no, i just posted the email of the indi that did...under the may 21 etc post
this is the reply i received'', margaret
did not reply...
fda response from my email sent the new official meeting date is May 21,2013...
bad bad bad fda...
email her...about possible coverup regarding class 3 devices...reason for meeting cancellation ???
i have sent some emails to the fda... let your voice be heard...
if this happened the fda is rolling right now and probably the reason for the meeting cancellation...
continuing to contact fda directory for names of contacts to get some action on this, join me the fda list all emails on their site...get active people it is r right...
what a joke u r
biel pr firm put pr april 1 with link to cover up, call 940-262-3584 , yahoo is not allowing the link to be posted ??? or call or email biel.
contact E&E communications biel pr firm at 940-262-3584 (yahoo is not allowing any links to be posted)
a former fda employee has uncovered a scandal that the fda appears to be covering up...etc.
this was sent out 4-1-13 by their pr firm read it , talks about a fda cover up annunced by a formaer fda employee...
fda site still not updated...
email to fda cotact just as i posted the email, no secrets here..
reschedule sp,, regardless fda cotact isn't sure why the delay was not posted on the fda site, they are looking into it...
Waterhouse, Jamie (Jamie.Waterhouse@fda.hhs.gov)
Add to contacts
9:57 AM
to: Michael DeMunbrun
This meeting has been postponed. I am not sure why it hasn't been updated online but we are looking into that issue.
Thanks,
Jamie
Jamie Mae Waterhouse
Health Science Administrator
FDA/CDRH/ODE/Medical Devices Advisory Committee
10903 New Hampshire Ave
White Oak Bldg 66
Silver Spring, MD 20993
301.796.3063 (Office)
Jamie.Waterhouse@fda.hhs.gov
well isn't this nice...WHAT'S UP DOC.
I like that word "intervening",,makes the mind work wonders as to what could possibly be occuring in this time space delay ???
and so we are locked with a large buy backlog...tug-o-war anyone !
this is where it all goes, thermal or not a thermal device, fda can't have both ways. (DJO Inc. device the Intelect -shortwave diathermy device approved class 2 several years ago by fda...).