FDA Inspection 881660 — Myerson LLC

Myerson LLC — FEI 3003928050

The FDA completed an inspection of Myerson LLC on June 6, 2014 in Chicago, 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
June 6, 2014
Fiscal Year
2014
Product Type
Devices
Project Area
Compliance: Devices
Location
Chicago, IL (United States)

Citations

IDCFRDescription
316821 CFR 820.198(a)Complaints
369621 CFR 820.100(b)Documentation