FDA Inspection 935425 — LifeSync Corporation

LifeSync Corporation — FEI 1000403400

The FDA completed an inspection of LifeSync Corporation on Jul 24, 2015 in Coral Springs, FL. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). 5 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Jul 24, 2015
Fiscal Year
2015
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Coral Springs, FL (United States)

Citations

IDCFRDescription
1471321 CFR 820.198(a)Lack of or inadequate complaint procedures
235021 CFR 820.25(b)Training - Lack of or inadequate procedures
310121 CFR 820.30(g)Design validation- Lack of or inadequate procedures
420821 CFR 806.20(a)Records not kept
47921 CFR 820.50Purchasing controls, Lack of or inadequate procedures