FDA Inspection 717683 — Pivotal Health Solutions

Pivotal Health Solutions — FEI 3008146957

The FDA completed an inspection of Pivotal Health Solutions on Jan 7, 2011 in Springfield, MO. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Jan 7, 2011
Fiscal Year
2011
Product Type
Devices
Project Area
Compliance: Devices
Location
Springfield, MO (United States)