FDA Inspection 844898 — Philips Healthcare

Philips Healthcare — FEI 3003888399

The FDA completed an inspection of Philips Healthcare on July 31, 2013 in San Diego, CA. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). Product area: Devices.

Inspection Details

Classification
Official Action Indicated (OAI) (OAI)
End Date
July 31, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
San Diego, CA (United States)