FDA Inspection 791490 — Stryker Medical Division Of Stryker Corporation

Stryker Medical Division Of Stryker Corporation — FEI 1831750

The FDA completed an inspection of Stryker Medical Division Of Stryker Corporation on Jun 26, 2012 in Portage, MI. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). 2 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Jun 26, 2012
Fiscal Year
2012
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Portage, MI (United States)

Citations

IDCFRDescription
337521 CFR 820.198(e)Records of complaint investigation
368021 CFR 820.70(a)Process control procedures, Lack of or inadequate procedures