Source: FDA record for this establishment. FDA publishes inspections or enforcement actions for this establishment, listed further down this page, but we have not matched this particular Form 483 to a document or an inspection date FDA has released. It stays out of the default view for that reason. To check it, open FDA's record for this establishment on FDA's Data Dashboard, listed under FEI 2518422.
Observations12
Issue DateJuly 01, 2010
StatusNo Warning Letter
Related Inspections10
Establishment Details
Firm
Philips Respironics, Inc.
Location
Murrysville, Pennsylvania, United States
FEI Number
2518422
Product Type
Devices
Issue Date
July 01, 2010
Country
United States
Inspection History, 2014 to 2022
NAI3
VAI2
OAI5
NAI means No Action Indicated. VAI means Voluntary Action Indicated. OAI means Official Action Indicated.