FDA PHILIPS RESPIRONICS CPAP DEVICE RECALL, INSPECTION & DOJ SUBPOENA CORRESPONDENCE

Original Request: Dear FDA: I am making a request under the Freedom of Information Act for documents related to the Philips Respironics June 2021 recall of millions of its BiBAP and CPAP obstructive sleep apnea devices. Specifically, I am requesting any communications between the FDA and Philips that relate to the inspection of the company’s Murrysville, PA facility between August 2021 and October 2021 – and any communications related to the subpoena the DOJ served Philips on April 8. I am also requesting any other correspondence between the FDA ETC
Tags: MedTech, Recall, 2021