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FDA Inspection 1010778 — Circadiance LLC

Circadiance LLC — FEI 3006182632

The FDA completed an inspection of Circadiance LLC on April 7, 2017 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 7, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Compliance: Devices
Location
Export, PA (United States)

Facility

Other inspections at this facility

  • 1098418 (NAI Wed Mar 20 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 816321 (NAI Wed Jan 30 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 709921 (NAI Wed Feb 16 2011 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 572951 (VAI Wed Apr 01 2009 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources