FDA Inspection 907062 — Smith & Nephew, Inc.

Smith & Nephew, Inc. — FEI 3006760724

The FDA completed an inspection of Smith & Nephew, Inc. on Jan 13, 2015 in Saint Petersburg, FL. 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
Jan 13, 2015
Fiscal Year
2015
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Saint Petersburg, FL (United States)

Citations

IDCFRDescription
1471321 CFR 820.198(a)Lack of or inadequate complaint procedures
313021 CFR 820.100(a)Lack of or inadequate procedures