FDA Inspection 551446 — Stryker Craniomaxillofacial Division
The FDA completed an inspection of Stryker Craniomaxillofacial Division on Dec 10, 2008 in Portage, MI. 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 10, 2008
- Fiscal Year
- 2009
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Portage, MI (United States)