FDA Inspection 876072 — Oximeter Plus, Inc

Oximeter Plus, Inc — FEI 3007176465

The FDA completed an inspection of Oximeter Plus, Inc on April 23, 2014 in Roslyn Heights, NY. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 2 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
April 23, 2014
Fiscal Year
2014
Product Type
Devices
Project Area
Compliance: Devices
Location
Roslyn Heights, NY (United States)

Citations

IDCFRDescription
313021 CFR 820.100(a)Lack of or inadequate procedures
328221 CFR 820.90(a)Nonconforming product, Lack of or inadequate procedures