FDA Inspection 674776 — Stryker Craniomaxillofacial Division
The FDA completed an inspection of Stryker Craniomaxillofacial Division on Aug 2, 2010 in Portage, MI. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Devices.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI)
- End Date
- Aug 2, 2010
- Fiscal Year
- 2010
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Portage, MI (United States)