FDA Inspection 695324 — Laurimed LLC

Laurimed LLC — FEI 3007209822

The FDA completed an inspection of Laurimed LLC on October 27, 2010 in Redwood City, CA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
October 27, 2010
Fiscal Year
2011
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Redwood City, CA (United States)

Citations

IDCFRDescription
323121 CFR 820.70(i)Documentation of software validation