FDA Inspection 871957 — Percussionaire Corporation

Percussionaire Corporation — FEI 1000524541

The FDA completed an inspection of Percussionaire Corporation on Feb 26, 2014 in Sandpoint, ID. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Feb 26, 2014
Fiscal Year
2014
Product Type
Devices
Project Area
Compliance: Devices
Location
Sandpoint, ID (United States)