FDA Inspection 831886 — Synthes, Inc.
The FDA completed an inspection of Synthes, Inc. on May 16, 2013 in West Chester, PA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.
Inspection Details
- Classification
- No Action Indicated (NAI) (NAI)
- End Date
- May 16, 2013
- Fiscal Year
- 2013
- Product Type
- Devices
- Project Area
- Bioresearch Monitoring
- Location
- West Chester, PA (United States)
Additional Details
Sponsor, Contract Research Organization