FDA Inspection 859106 — Synthes, Inc.

Synthes, Inc. — FEI 3005180112

The FDA completed an inspection of Synthes, Inc. on November 13, 2013 in West Chester, PA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
November 13, 2013
Fiscal Year
2014
Product Type
Devices
Project Area
Compliance: Devices
Location
West Chester, PA (United States)

Citations

IDCFRDescription
369621 CFR 820.100(b)Documentation