FDA Inspection 1106099 — Pressure Point Inc

Pressure Point Inc — FEI 3009441145

The FDA completed an inspection of Pressure Point Inc on May 3, 2019 in Tinton Falls, NJ. 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
May 3, 2019
Fiscal Year
2019
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Tinton Falls, NJ (United States)