FDA Inspection 572951 — Circadiance LLC

Circadiance LLC — FEI 3006182632

The FDA completed an inspection of Circadiance LLC on April 1, 2009 in Export, PA. 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
April 1, 2009
Fiscal Year
2009
Product Type
Devices
Project Area
Compliance: Devices
Location
Export, PA (United States)