Fisher Wallace Laboratories Amends Citizen Petition

January 17, 2017 – Following a comment from the Director of the FDA’s Office of Scientific Integrity, Fisher Wallace amended its citizen petition to the FDA in regards to reclassification of its Cranial Electrical Stimulators, believing that OSI failed to address the majority of the complaints in the citizen petition.  The company requested that the FDA conduct a more thorough review of its citizen petition.  The docket number for the citizen petition is FDA-2012-P-0260-0001/CP.

By: Joyce L. Nadipuram