FDA Inspection 576581 — Smith & Nephew, Inc.

Smith & Nephew, Inc. — FEI 1020279

The FDA completed an inspection of Smith & Nephew, Inc. on April 23, 2009 in Memphis, TN. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). 3 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
April 23, 2009
Fiscal Year
2009
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Memphis, TN (United States)

Citations

IDCFRDescription
320121 CFR 820.40(a)Not approved or obsolete document retrieval
369021 CFR 820.100(a)(3)Identification of actions needed
418921 CFR 820.198(a)General