03/11/2019
https://congress.gov...
"Yet FDA has shared with me that the agency physically examined only 5,564 of them."
"I also understand that my colleagues and industry stakeholders still would like to see preemption language added to this legislation."
"That's unacceptable, but unless we equip FDA with the tools and resources the agency needs, we're going to continue to see frightening issues with these products for years to come."
"These are all giant gaps in consumer safety that we have to address."