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FDA Inspection 679200 — Peter Schiff Enterprises

Peter Schiff Enterprises — FEI 1000112898

The FDA completed an inspection of Peter Schiff Enterprises on August 30, 2010 in Cookeville, TN. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). Product area: Devices.

Inspection Details

Classification
Official Action Indicated (OAI) (OAI)
End Date
August 30, 2010
Fiscal Year
2010
Product Type
Devices
Project Area
Compliance: Devices
Location
Cookeville, TN (United States)

Facility

Other inspections at this facility

  • 1008504 (VAI Thu Apr 13 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 825133 (VAI Fri Apr 12 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 756724 (VAI Wed Dec 07 2011 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources