FDA Inspection 870927 — Perry Dynamics Inc

Perry Dynamics Inc — FEI 3004979815

The FDA completed an inspection of Perry Dynamics Inc on March 19, 2014 in Decatur, IL. 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
March 19, 2014
Fiscal Year
2014
Product Type
Devices
Project Area
Compliance: Devices
Location
Decatur, IL (United States)

Citations

IDCFRDescription
315521 CFR 820.181(a)DMR device specifications
315921 CFR 820.184DHR content