FDA Inspection 684637 — LifeSync Corporation

LifeSync Corporation — FEI 1000403400

The FDA completed an inspection of LifeSync Corporation on Oct 15, 2010 in Coral Springs, 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
Oct 15, 2010
Fiscal Year
2011
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Coral Springs, FL (United States)

Citations

IDCFRDescription
312721 CFR 820.80(e)Documentation
368021 CFR 820.70(a)Process control procedures, Lack of or inadequate procedures