FDA Inspection 1342212 — Jones Medical Instrument Co.

Jones Medical Instrument Co. — FEI 1416588

The FDA completed an inspection of Jones Medical Instrument Co. on Oct 15, 2026 in Oak Brook, IL. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Oct 15, 2026
Fiscal Year
2027
Product Type
Devices
Project Area
Compliance: Devices
Location
Oak Brook, IL (United States)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.