FDA Inspection 1027770 — Scottcare Corporation

Scottcare Corporation — FEI 1527715

The FDA completed an inspection of Scottcare Corporation on October 5, 2017 in Cleveland, OH. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 3 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
October 5, 2017
Fiscal Year
2018
Product Type
Devices
Project Area
Compliance: Devices
Location
Cleveland, OH (United States)

Citations

IDCFRDescription
312121 CFR 820.80(b)Lack of or inadequate receiving acceptance procedures
319221 CFR 820.30(g)Design validation - user needs and intended uses
328221 CFR 820.90(a)Nonconforming product, Lack of or inadequate procedures