FDA Inspection 609250 — Aspyra, LLC

Aspyra, LLC — FEI 3001452787

The FDA completed an inspection of Aspyra, LLC on Apr 8, 2009 in Jacksonville, FL. 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
Apr 8, 2009
Fiscal Year
2009
Product Type
Devices
Project Area
Compliance: Devices
Location
Jacksonville, FL (United States)