FDA Inspection 1117670 — Physiq Inc.

Physiq Inc. — FEI 3013414924

The FDA completed an inspection of Physiq Inc. on December 18, 2019 in Chicago, 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
December 18, 2019
Fiscal Year
2020
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Chicago, IL (United States)