FDA Inspection 903227 — Jones Medical Instrument Co.

Jones Medical Instrument Co. — FEI 1416588

The FDA completed an inspection of Jones Medical Instrument Co. on November 13, 2014 in Oak Brook, IL. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). 2 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
November 13, 2014
Fiscal Year
2015
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Oak Brook, IL (United States)

Citations

IDCFRDescription
235021 CFR 820.25(b)Training - Lack of or inadequate procedures
316021 CFR 820.184Lack of or inadequate DHR procedures