FDA Inspection 1107051 — Physio PS, Inc.

Physio PS, Inc. — FEI 3000210032

The FDA completed an inspection of Physio PS, Inc. on June 12, 2019 in Londonderry, NH. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
June 12, 2019
Fiscal Year
2019
Product Type
Devices
Project Area
Compliance: Devices
Location
Londonderry, NH (United States)