FDA Inspection 1061408 — Prytime Medical Devices, Inc.

Prytime Medical Devices, Inc. — FEI 3012279212

The FDA completed an inspection of Prytime Medical Devices, Inc. on Jul 17, 2018 in Lakewood, CO. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.