FDA Inspection 898177 — Natus Medical Incorporated

Natus Medical Incorporated — FEI 3018859

The FDA completed an inspection of Natus Medical Incorporated on September 10, 2014 in Seattle, WA. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). 7 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Official Action Indicated (OAI) (OAI)
End Date
September 10, 2014
Fiscal Year
2014
Product Type
Devices
Project Area
Compliance: Devices
Location
Seattle, WA (United States)

Citations

IDCFRDescription
1471321 CFR 820.198(a)Lack of or inadequate complaint procedures
1471621 CFR 820.30(f)Design verification - output does not meet input requirement
310121 CFR 820.30(g)Design validation- Lack of or inadequate procedures
310421 CFR 820.30(j)Design history file
313021 CFR 820.100(a)Lack of or inadequate procedures
333121 CFR 820.181DMR - not or inadequately maintained
369621 CFR 820.100(b)Documentation