REPORTING NEUROMONICS OASIS TO THE FDA
Reporting Neuromonics Oasis to the FDA
For those who have had similar negative experiences with the Neuromonics Oasis device, please consider lodging a complaint with the U.S. Food and Drug Administration (FDA).
An online reporting form entitled “MedWatch Online Voluntary Reporting Form (3500),” can be located at:
https://www.accessdata.fda.gov/scripts/medwatch/
Regards,
Ed W.
For those who have had similar negative experiences with the Neuromonics Oasis device, please consider lodging a complaint with the U.S. Food and Drug Administration (FDA).
An online reporting form entitled “MedWatch Online Voluntary Reporting Form (3500),” can be located at:
https://www.accessdata.fda.gov/scripts/medwatch/
Regards,
Ed W.
Labels: Dr. Michael L. Hill, FDA, neuromonics, oasis, ringing, tinnitus
posted by Neuromonics-danger at
5:46 PM
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