FDA Inspection 1028932 — Jones Medical Instrument Co.

Jones Medical Instrument Co. — FEI 1416588

The FDA completed an inspection of Jones Medical Instrument Co. on September 19, 2017 in Oak Brook, IL. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
September 19, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Compliance: Devices
Location
Oak Brook, IL (United States)