FDA Inspection 999003 — Joint Jack Company

Joint Jack Company — FEI 1000159372

The FDA completed an inspection of Joint Jack Company on Jan 12, 2017 in Glastonbury, CT. 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
Jan 12, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Compliance: Devices
Location
Glastonbury, CT (United States)