FDA Inspection 1073570 — Philips North America, LLC
The FDA completed an inspection of Philips North America, LLC on Dec 4, 2018 in Andover, MA. The inspection was classified OAI (Official Action Indicated — regulatory and/or administrative actions are recommended). Product area: Devices.
Inspection Details
- Classification
- Official Action Indicated (OAI)
- End Date
- Dec 4, 2018
- Fiscal Year
- 2019
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Andover, MA (United States)