FDA Inspection 1024164 — DePuy Orthopaedics, Inc.

DePuy Orthopaedics, Inc. — FEI 1818910

The FDA completed an inspection of DePuy Orthopaedics, Inc. on September 1, 2017 in Warsaw, IN. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). 2 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
September 1, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Warsaw, IN (United States)

Citations

IDCFRDescription
313021 CFR 820.100(a)Lack of or inadequate procedures
328221 CFR 820.90(a)Nonconforming product, Lack of or inadequate procedures